Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8419 |
|---|---|
| ensemblid | ENSG00000170819.5 |
| hgncid | 1041 |
| symbol | BFSP2 |
| name | beaded filament structural protein 2 |
| refseq_nuc | NM_003571.4 |
| refseq_prot | NP_003562.1 |
| ensembl_nuc | ENST00000302334.3 |
| ensembl_prot | ENSP00000304987.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 133400056 |
| end | 133475208 |
| strand | + |
| ver | v1.2 |
| region | chr3:133400056-133475208 |
| region5000 | chr3:133395056-133480208 |
| regionname0 | BFSP2_chr3_133400056_133475208 |
| regionname5000 | BFSP2_chr3_133395056_133480208 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 415 | 263 | 80 | 52 | 90 | 8 | 31 | 65 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0002 | 0/0 | 415 | 9 | 1 | 2 | 2 | 2 | 2 | 2 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0003 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0004 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0005 | 0/0 | 415 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0006 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1248 | 163 | 71 | 35 | 41 | 3 | 12 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0002 | 0/1 | 1248 | 97 | 7 | 17 | 49 | 5 | 18 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0003 | 0/0 | 1248 | 8 | 1 | 2 | 2 | 2 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0004 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0005 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0006 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0007 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0008 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0009 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| c0010 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 265 | 275 | 82 | 54 | 93 | 10 | 34 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| t0002 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1248 | 163 | 71 | 35 | 41 | 3 | 12 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0002 | 0/1 | 1248 | 97 | 7 | 17 | 49 | 5 | 18 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0004 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0008 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0002c0003 | 0/0 | 1248 | 8 | 1 | 2 | 2 | 2 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0002c0007 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0003c0010 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0004c0005 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0005c0006 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0006c0009 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1512 | 163 | 71 | 35 | 41 | 3 | 12 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0002t0001 | 0/1 | 1512 | 96 | 7 | 17 | 48 | 5 | 18 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0002t0002 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0004t0001 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0001c0008t0001 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0002c0003t0001 | 0/0 | 1512 | 8 | 1 | 2 | 2 | 2 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0002c0007t0001 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0003c0010t0001 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0004c0005t0001 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0005c0006t0001 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| a0006c0009t0001 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | copy fasta | chr3 | 133395056 | 133480208 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0008t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0003c0010t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0004c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0005c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0006c0009t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0215 | EUR | GBR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00558 | hp2 | a0003 | c0010 | t0001 | g0156 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0252 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0222 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0172 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0145 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0220 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02738 | hp1 | a0002 | c0007 | t0001 | g0236 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0255 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03654 | hp1 | a0001 | c0008 | t0001 | g0125 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04204 | hp2 | a0005 | c0006 | t0001 | g0264 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18952 | hp1 | a0004 | c0005 | t0001 | g0092 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19030 | hp1 | a0006 | c0009 | t0001 | g0167 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0084 | EUR | TSI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0154 | EUR | TSI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | GIH | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | GIH | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0107 | REF | REF | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400462
|
C | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.379C>G | p.Gln127Glu | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 407/1512 | 379/1248 | 127/415 | chr3 | 133400462 | ||
| chr3:133400493
|
G | A | 1 | a0004 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.410G>A | p.Arg137Gln | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 438/1512 | 410/1248 | 137/415 | chr3 | 133400493 | ||
| chr3:133400520
|
G | A | 1 | a0005 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.437G>A | p.Arg146His | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 465/1512 | 437/1248 | 146/415 | chr3 | 133400520 | ||
| chr3:133447350
|
A | G | 1 | a0006 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.523A>G | p.Met175Val | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/7 | 551/1512 | 523/1248 | 175/415 | chr3 | 133447350 | ||
| chr3:133472541
|
C | A | 2 | a0002a0005 | 10 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(7): Show |
missense_variant | MODERATE | c.1220C>A | p.Ala407Asp | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/7 | 1248/1512 | 1220/1248 | 407/415 | chr3 | 133472541 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400245
|
C | T | 1 | a0001c0004 | 2 | HG03098.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.162C>T | p.Pro54Pro | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 190/1512 | 162/1248 | 54/415 | chr3 | 133400245 | ||
| chr3:133400452
|
C | T | 1 | a0001c0004 | 2 | HG03098.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.369C>T | p.His123His | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 397/1512 | 369/1248 | 123/415 | chr3 | 133400452 | ||
| chr3:133448519
|
G | A | 4 | a0001c0002a0001c0008a0002c0007others(1): Show | 100 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
synonymous_variant | LOW | c.603G>A | p.Ala201Ala | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/7 | 631/1512 | 603/1248 | 201/415 | chr3 | 133448519 | ||
| chr3:133448636
|
C | T | 1 | a0001c0008 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.720C>T | p.Asn240Asn | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/7 | 748/1512 | 720/1248 | 240/415 | chr3 | 133448636 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133475007
|
C | T | 1 | a0001c0002t0002 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 7/7 | 35 | chr3 | 133475007 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400782
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(129): Show | 137 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.489+210G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400782 | ||||||
| chr3:133400858
|
A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0040others(97): Show | 102 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.489+286A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400858 | ||||||
| chr3:133400886
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(10): Show | 16 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.489+314G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400886 | ||||||
| chr3:133401437
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+865T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133401437 | ||||||
| chr3:133401512
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+940T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133401512 | ||||||
| chr3:133402236
|
A | G | 2 | a0001c0004t0001g0033a0001c0004t0001g0034 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.489+1664A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402236 | ||||||
| chr3:133402452
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1880A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402452 | ||||||
| chr3:133402497
|
G | A | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.489+1925G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402497 | ||||||
| chr3:133402511
|
TG | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA18522.hp2 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.489+1942delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133402511 | |||||
| chr3:133402584
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+2012T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402584 | ||||||
| chr3:133402643
|
C | CT | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(24): Show | 30 | HG01175.hp1 HG01255.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.489+2086dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133402643 | |||||
| chr3:133402758
|
A | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0036others(86): Show | 91 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.489+2186A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402758 | ||||||
| chr3:133402761
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(25): Show | 31 | HG01175.hp1 HG01255.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.489+2189G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402761 | ||||||
| chr3:133402786
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.489+2214G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402786 | ||||||
| chr3:133402797
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+2225C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402797 | ||||||
| chr3:133402972
|
C | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2400C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402972 | ||||||
| chr3:133403364
|
C | A | 18 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(15): Show | 18 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2792C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403364 | ||||||
| chr3:133403364
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+2792C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403364 | ||||||
| chr3:133403372
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(43): Show | 49 | HG00738.hp2 HG01175.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.489+2800A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403372 | ||||||
| chr3:133403785
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(259): Show | 267 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.489+3213T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403785 | ||||||
| chr3:133403961
|
C | T | 2 | a0001c0002t0001g0131a0001c0002t0001g0132 | 2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.489+3389C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403961 | ||||||
| chr3:133403998
|
GA | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(143): Show | 148 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.489+3428delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133403998 | |||||
| chr3:133404086
|
G | A | 2 | a0001c0004t0001g0033a0001c0004t0001g0034 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.489+3514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404086 | ||||||
| chr3:133404113
|
G | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0002t0001g0243others(1): Show | 4 | NA18956.hp2 NA18969.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3541G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404113 | ||||||
| chr3:133404419
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.489+3847C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404419 | ||||||
| chr3:133404443
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(36): Show | 42 | HG00738.hp2 HG01175.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.489+3871A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404443 | ||||||
| chr3:133404801
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+4229A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404801 | ||||||
| chr3:133404842
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489+4270C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404842 | ||||||
| chr3:133404892
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 143 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.489+4320G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404892 | ||||||
| chr3:133405113
|
T | A | 2 | a0001c0002t0001g0016a0001c0004t0001g0033 | 2 | HG03579.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.489+4541T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405113 | ||||||
| chr3:133405205
|
C | T | 15 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0001g0129others(12): Show | 15 | HG01891.hp1 HG02056.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+4633C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405205 | ||||||
| chr3:133405519
|
C | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+4947C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405519 | ||||||
| chr3:133405741
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+5169G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405741 | ||||||
| chr3:133405755
|
C | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(11): Show | 17 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+5183C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405755 | ||||||
| chr3:133405812
|
G | A | 1 | a0003c0010t0001g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.489+5240G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405812 | ||||||
| chr3:133405878
|
A | C | 1 | a0001c0004t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.489+5306A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405878 | ||||||
| chr3:133405878
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 10 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5306A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405878 | ||||||
| chr3:133405921
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 10 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+5349C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405921 | ||||||
| chr3:133405982
|
G | A | 1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+5410G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405982 | ||||||
| chr3:133406020
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0002t0001g0039 | 3 | HG01346.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.489+5448G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406020 | ||||||
| chr3:133406098
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.489+5526C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406098 | ||||||
| chr3:133406114
|
C | CT | 9 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 11 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+5543dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406114 | |||||
| chr3:133406116
|
A | AT | 111 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(108): Show | 113 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.489+5558dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406116 | |||||
| chr3:133406116
|
A | ATT | 10 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0112others(7): Show | 10 | HG01081.hp2 HG02738.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5557_489+5558d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406116 | |||||
| chr3:133406116
|
A | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 11 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+5544A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406116 | ||||||
| chr3:133406141
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(12): Show | 18 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.489+5569T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406141 | ||||||
| chr3:133406144
|
A | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.489+5572A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406144 | ||||||
| chr3:133406327
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.489+5755G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406327 | ||||||
| chr3:133406371
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.489+5799C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406371 | ||||||
| chr3:133406560
|
GCCATCTA others(4): Show |
G | 6 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5991_489+6001d others(13): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406560 | |||||
| chr3:133406604
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+6032C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406604 | ||||||
| chr3:133406753
|
G | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 30 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.489+6181G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406753 | ||||||
| chr3:133406841
|
A | G | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.489+6269A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406841 | ||||||
| chr3:133406869
|
A | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(113): Show | 119 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.489+6297A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406869 | ||||||
| chr3:133406896
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.489+6324G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406896 | ||||||
| chr3:133406967
|
G | A | 11 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0002t0001g0120others(8): Show | 11 | HG02056.hp1 HG02129.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+6395G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406967 | ||||||
| chr3:133407666
|
C | T | 2 | a0001c0001t0001g0110a0001c0002t0001g0111 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.489+7094C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407666 | ||||||
| chr3:133407710
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.489+7138A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407710 | ||||||
| chr3:133407809
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.489+7237C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407809 | ||||||
| chr3:133407888
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+7316T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407888 | ||||||
| chr3:133408092
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 9 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+7520A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408092 | ||||||
| chr3:133408113
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+7541T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408113 | ||||||
| chr3:133408138
|
C | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(73): Show | 78 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.489+7566C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408138 | ||||||
| chr3:133408186
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 11 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+7614A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408186 | ||||||
| chr3:133408190
|
CTCTTTTA others(11): Show |
C | 1 | a0001c0002t0001g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.489+7620_489+7637d others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133408190 | |||||
| chr3:133408611
|
A | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0002t0001g0107 | 3 | HG03239.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.489+8039A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408611 | ||||||
| chr3:133408668
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.489+8096G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408668 | ||||||
| chr3:133408821
|
T | TG | 79 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0036others(76): Show | 81 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.489+8250dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133408821 | |||||
| chr3:133408908
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0149 | 3 | HG02615.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.489+8336G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408908 | ||||||
| chr3:133409114
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG01081.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+8542A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409114 | ||||||
| chr3:133409166
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.489+8594C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409166 | ||||||
| chr3:133409227
|
G | GGT | 125 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0030others(122): Show | 125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.489+8684_489+8685d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGT | 12 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(9): Show | 13 | HG01175.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+8682_489+8685d others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGTGT | 83 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0040others(80): Show | 85 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.489+8680_489+8685d others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 15 | HG01081.hp1 HG01081.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+8678_489+8685d others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGTGTG others(3): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0017others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+8676_489+8685d others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGTGTG others(5): Show |
1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+8674_489+8685d others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409227
|
G | GGTGTGTG others(7): Show |
9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+8672_489+8685d others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | |||||
| chr3:133409286
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+8714T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409286 | ||||||
| chr3:133409380
|
T | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(103): Show | 108 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.489+8808T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409380 | ||||||
| chr3:133409605
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 135 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.489+9033T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409605 | ||||||
| chr3:133409634
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+9062C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409634 | ||||||
| chr3:133409704
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+9132C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409704 | ||||||
| chr3:133410099
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.489+9527T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410099 | ||||||
| chr3:133410260
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.489+9688C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410260 | ||||||
| chr3:133410310
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.489+9738T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410310 | ||||||
| chr3:133410428
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(90): Show | 95 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.489+9856C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410428 | ||||||
| chr3:133410491
|
C | T | 1 | a0002c0007t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.489+9919C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410491 | ||||||
| chr3:133411061
|
C | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(77): Show | 84 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.489+10489C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411061 | ||||||
| chr3:133411108
|
T | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(75): Show | 80 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.489+10536T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411108 | ||||||
| chr3:133411154
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.489+10582T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411154 | ||||||
| chr3:133411179
|
C | T | 2 | a0001c0001t0001g0030a0001c0002t0001g0031 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.489+10607C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411179 | ||||||
| chr3:133411180
|
GA | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0022others(38): Show | 41 | HG00738.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.489+10627delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | |||||
| chr3:133411180
|
GAA | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 134 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.489+10626_489+1062 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | |||||
| chr3:133411180
|
GAAA | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(22): Show | 27 | HG00099.hp2 HG00438.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.489+10625_489+1062 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | |||||
| chr3:133411180
|
GAAAA | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0023others(62): Show | 67 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.489+10624_489+1062 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | |||||
| chr3:133411199
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0256 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.489+10627A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411199 | ||||||
| chr3:133411573
|
A | C | 1 | a0001c0002t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+11001A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411573 | ||||||
| chr3:133411625
|
A | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0040others(32): Show | 37 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.489+11053A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411625 | ||||||
| chr3:133411721
|
CA | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 257 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.489+11151delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411721 | |||||
| chr3:133411729
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.489+11157C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411729 | ||||||
| chr3:133411934
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+11362T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411934 | ||||||
| chr3:133412004
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+11432G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412004 | ||||||
| chr3:133412005
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.489+11433A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412005 | ||||||
| chr3:133412026
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.489+11454C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412026 | ||||||
| chr3:133412035
|
C | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.489+11463C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412035 | ||||||
| chr3:133412044
|
G | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(7): Show | 10 | HG02257.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+11472G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412044 | ||||||
| chr3:133412080
|
C | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149others(4): Show | 7 | HG01258.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+11508C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412080 | ||||||
| chr3:133412161
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11589C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412161 | ||||||
| chr3:133412456
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+11884C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412456 | ||||||
| chr3:133412572
|
T | C | 2 | a0001c0002t0001g0124a0001c0008t0001g0125 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.489+12000T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412572 | ||||||
| chr3:133412618
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+12046G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412618 | ||||||
| chr3:133412784
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.489+12212G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412784 | ||||||
| chr3:133412872
|
G | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0241others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12300G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412872 | ||||||
| chr3:133413037
|
C | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+12465C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413037 | ||||||
| chr3:133413055
|
T | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(7): Show | 10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+12483T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413055 | ||||||
| chr3:133413149
|
T | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0241others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12577T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413149 | ||||||
| chr3:133413182
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0241others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12610G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413182 | ||||||
| chr3:133413208
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(7): Show | 10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+12636C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413208 | ||||||
| chr3:133413335
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+12763C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413335 | ||||||
| chr3:133413353
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+12781C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413353 | ||||||
| chr3:133413652
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.489+13080G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413652 | ||||||
| chr3:133413845
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+13273T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413845 | ||||||
| chr3:133413846
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+13274A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413846 | ||||||
| chr3:133413953
|
C | T | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+13381C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413953 | ||||||
| chr3:133414035
|
CCT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+13469_489+1347 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414035 | |||||
| chr3:133414243
|
CCT | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+13672_489+1367 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414243 | ||||||
| chr3:133414251
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.489+13679G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414251 | ||||||
| chr3:133414269
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.489+13697G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414269 | ||||||
| chr3:133414281
|
TACTC | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0032others(19): Show | 22 | HG01123.hp2 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.489+13712_489+1371 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414281 | |||||
| chr3:133414717
|
A | ATCCCCTC others(42): Show |
1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+14166_489+1416 others(53): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | |||||
| chr3:133414717
|
A | ATCCCCTC others(41): Show |
9 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(6): Show | 9 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | |||||
| chr3:133414717
|
A | ATCCCCTC others(41): Show |
20 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00639.hp1 HG02109.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | |||||
| chr3:133414717
|
A | ATCCCCTC others(65): Show |
215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 220 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(76): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | |||||
| chr3:133414717
|
A | ATCTCCTC others(41): Show |
24 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0018others(21): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+14147_489+1414 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | |||||
| chr3:133414786
|
AC | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(40): Show | 43 | HG00621.hp2 HG00639.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.489+14224delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414786 | |||||
| chr3:133414786
|
ACC | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 200 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.489+14223_489+1422 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414786 | |||||
| chr3:133414792
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.489+14220C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414792 | ||||||
| chr3:133414853
|
A | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(7): Show | 10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+14281A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414853 | ||||||
| chr3:133414863
|
ACCTGCCC others(17): Show |
A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+14296_489+1431 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414863 | |||||
| chr3:133414958
|
CCCTCTAC others(17): Show |
C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.489+14400_489+1442 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414958 | |||||
| chr3:133415061
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(7): Show | 10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+14489C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415061 | ||||||
| chr3:133415068
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+14496C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415068 | ||||||
| chr3:133415220
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489+14648C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415220 | ||||||
| chr3:133415222
|
CCTCACCT others(467): Show |
C | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+14657_489+1513 others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415222 | |||||
| chr3:133415229
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(226): Show | 234 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.489+14657T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415229 | ||||||
| chr3:133415274
|
A | ACCCTTGC others(5): Show |
1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14705_489+1470 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415274 | |||||
| chr3:133415286
|
A | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14714A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415286 | ||||||
| chr3:133415290
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+14718T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415290 | ||||||
| chr3:133415293
|
C | T | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14721C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415293 | ||||||
| chr3:133415297
|
C | T | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14725C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415297 | ||||||
| chr3:133415310
|
G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14738G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415310 | ||||||
| chr3:133415314
|
C | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14742C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415314 | ||||||
| chr3:133415321
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 16 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.489+14749T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415321 | ||||||
| chr3:133415338
|
G | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14766G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415338 | ||||||
| chr3:133415341
|
T | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14769T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415341 | ||||||
| chr3:133415348
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(69): Show | 74 | HG00099.hp2 HG00621.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.489+14776C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415348 | ||||||
| chr3:133415351
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(69): Show | 74 | HG00099.hp2 HG00621.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.489+14779T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415351 | ||||||
| chr3:133415351
|
T | TCTACTCA others(17): Show |
185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(182): Show | 188 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.489+14791_489+1479 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415351 | |||||
| chr3:133415482
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+14910C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415482 | ||||||
| chr3:133415549
|
CCTCTACT others(17): Show |
C | 20 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0083others(17): Show | 20 | HG00621.hp2 HG00738.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+15016_489+1503 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415549 | |||||
| chr3:133415572
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15000C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415572 | ||||||
| chr3:133415596
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15024C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415596 | ||||||
| chr3:133415617
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.489+15045C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415617 | ||||||
| chr3:133415676
|
TCCCCTCT others(5): Show |
T | 21 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0069others(18): Show | 21 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+15122_489+1513 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415676 | |||||
| chr3:133415703
|
CCT | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+15132_489+1513 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415703 | ||||||
| chr3:133415967
|
G | T | 1 | a0001c0002t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+15395G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415967 | ||||||
| chr3:133415987
|
CT | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0175a0001c0001t0001g0256 | 3 | HG02451.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.489+15416delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415987 | ||||||
| chr3:133416012
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+15440G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416012 | ||||||
| chr3:133416033
|
CCT | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15462_489+1546 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416033 | ||||||
| chr3:133416119
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489+15547T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416119 | ||||||
| chr3:133416161
|
CCTCTCCC others(17): Show |
C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.489+15599_489+1562 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416161 | |||||
| chr3:133416249
|
TCCCCTGT others(17): Show |
T | 2 | a0001c0001t0001g0026a0002c0003t0001g0145 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.489+15690_489+1571 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416249 | |||||
| chr3:133416295
|
T | C | 1 | a0002c0003t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.489+15723T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416295 | ||||||
| chr3:133416312
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.489+15740C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416312 | ||||||
| chr3:133416325
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+15753G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416325 | ||||||
| chr3:133416363
|
A | G | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15791A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416363 | ||||||
| chr3:133416398
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0002t0001g0077 | 3 | HG00438.hp2 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.489+15826C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416398 | ||||||
| chr3:133416405
|
C | T | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+15833C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416405 | ||||||
| chr3:133416436
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(266): Show | 274 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.489+15864G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416436 | ||||||
| chr3:133416459
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01099.hp2 HG02109.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.489+15887T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416459 | ||||||
| chr3:133416516
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+15944C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416516 | ||||||
| chr3:133416574
|
AC | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+16006delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416574 | |||||
| chr3:133416580
|
TCCATCTC others(17): Show |
T | 1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+16020_489+1604 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416580 | |||||
| chr3:133416633
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+16061C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416633 | ||||||
| chr3:133416766
|
C | T | 19 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0083others(16): Show | 19 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+16194C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416766 | ||||||
| chr3:133416821
|
C | CCTCTCCC others(17): Show |
24 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0018others(21): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+16256_489+1625 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416821 | |||||
| chr3:133416979
|
C | T | 5 | a0001c0002t0001g0076a0001c0002t0001g0089a0001c0002t0001g0206others(2): Show | 5 | NA18947.hp2 NA18952.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+16407C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416979 | ||||||
| chr3:133417035
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0127a0001c0001t0001g0198 | 3 | NA18946.hp1 NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.489+16463C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417035 | ||||||
| chr3:133417092
|
C | CTCTCCCC others(17): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0212a0001c0002t0001g0044 | 3 | NA18993.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.489+16534_489+1655 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417092 | |||||
| chr3:133417132
|
C | T | 1 | a0001c0002t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+16560C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417132 | ||||||
| chr3:133417138
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+16566C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417138 | ||||||
| chr3:133417165
|
C | G | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+16593C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417165 | ||||||
| chr3:133417176
|
T | G | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16604T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417176 | ||||||
| chr3:133417206
|
CGCCTCTC others(17): Show |
C | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16635_489+1665 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417206 | ||||||
| chr3:133417231
|
T | A | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16659T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417231 | ||||||
| chr3:133417279
|
CCCTCTCC others(17): Show |
C | 1 | a0001c0001t0001g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.489+16712_489+1673 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417279 | |||||
| chr3:133417285
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149 | 3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+16713C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417285 | ||||||
| chr3:133417309
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0137others(1): Show | 4 | HG02257.hp1 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+16737C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417309 | ||||||
| chr3:133417309
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.489+16737C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417309 | ||||||
| chr3:133417373
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.489+16801C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417373 | ||||||
| chr3:133417443
|
A | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0127a0001c0001t0001g0198 | 3 | NA18946.hp1 NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.489+16871A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417443 | ||||||
| chr3:133417524
|
C | CCCA | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 129 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.489+16953_489+1695 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417524 | |||||
| chr3:133417592
|
CCCTCTAC others(5): Show |
C | 15 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 15 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+17036_489+1704 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417592 | |||||
| chr3:133417594
|
C | CTCTACTC others(24): Show |
1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.489+17025_489+1705 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417594 | |||||
| chr3:133417674
|
T | C | 1 | a0001c0002t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.489+17102T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417674 | ||||||
| chr3:133417677
|
T | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0025others(17): Show | 22 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.489+17105T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417677 | ||||||
| chr3:133417747
|
C | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0018others(21): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+17175C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417747 | ||||||
| chr3:133417831
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.489+17259T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417831 | ||||||
| chr3:133417839
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.489+17267C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417839 | ||||||
| chr3:133417843
|
C | T | 2 | a0001c0001t0001g0134a0001c0002t0001g0111 | 2 | NA18970.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.489+17271C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417843 | ||||||
| chr3:133417843
|
CGTCCTCT others(17): Show |
C | 2 | a0001c0002t0001g0150a0001c0002t0001g0151 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.489+17317_489+1734 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417843 | |||||
| chr3:133417858
|
AC | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+17287delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417858 | ||||||
| chr3:133418007
|
ATTCTACT others(101): Show |
A | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+17469_489+1757 others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418007 | |||||
| chr3:133418022
|
GTCCTCTC others(17): Show |
G | 20 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0083others(17): Show | 20 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+17469_489+1749 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418022 | |||||
| chr3:133418032
|
CTCTACTC others(77): Show |
C | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+17469_489+1755 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418032 | |||||
| chr3:133418046
|
ATCCTCTC others(77): Show |
A | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489+17498_489+1758 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418046 | |||||
| chr3:133418089
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0070others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+17517C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418089 | ||||||
| chr3:133418095
|
A | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0025others(28): Show | 33 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.489+17523A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418095 | ||||||
| chr3:133418244
|
T | C | 39 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(36): Show | 39 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.489+17672T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418244 | ||||||
| chr3:133418355
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 37 | HG00639.hp1 HG00639.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.489+17783C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418355 | ||||||
| chr3:133418440
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 178 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.489+17868G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418440 | ||||||
| chr3:133418579
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0055others(28): Show | 31 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.489+18007T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418579 | ||||||
| chr3:133418590
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 175 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.489+18018G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418590 | ||||||
| chr3:133418710
|
C | A | 12 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0074others(9): Show | 13 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+18138C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418710 | ||||||
| chr3:133418820
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.489+18248A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418820 | ||||||
| chr3:133418843
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.489+18271G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418843 | ||||||
| chr3:133418982
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.489+18410C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418982 | ||||||
| chr3:133419132
|
A | ATCTGTGT others(4699): Show |
1 | a0001c0002t0001g0243 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.489+18695_489+1869 others(4710): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133419132 | |||||
| chr3:133419146
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+18574T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419146 | ||||||
| chr3:133419192
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(106): Show | 112 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.489+18620G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419192 | ||||||
| chr3:133419268
|
C | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 182 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.489+18696C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419268 | ||||||
| chr3:133419318
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+18746C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419318 | ||||||
| chr3:133419351
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+18779G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419351 | ||||||
| chr3:133419459
|
C | A | 2 | a0001c0001t0001g0112a0001c0004t0001g0033 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.489+18887C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419459 | ||||||
| chr3:133419495
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 182 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.489+18923T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419495 | ||||||
| chr3:133419636
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0148a0001c0001t0001g0256others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+19064C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419636 | ||||||
| chr3:133419834
|
A | G | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+19262A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419834 | ||||||
| chr3:133419922
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0055others(26): Show | 29 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+19350C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419922 | ||||||
| chr3:133419944
|
C | T | 2 | a0001c0002t0001g0131a0001c0002t0001g0205 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.489+19372C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419944 | ||||||
| chr3:133420134
|
G | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 183 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.489+19562G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420134 | ||||||
| chr3:133420166
|
T | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0099others(7): Show | 10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+19594T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420166 | ||||||
| chr3:133420409
|
G | T | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.489+19837G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420409 | ||||||
| chr3:133420553
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+19981A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420553 | ||||||
| chr3:133420601
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.489+20029C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420601 | ||||||
| chr3:133420628
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 183 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.489+20056A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420628 | ||||||
| chr3:133420730
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0256 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.489+20158C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420730 | ||||||
| chr3:133420941
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489+20369C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420941 | ||||||
| chr3:133421002
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.489+20430C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421002 | ||||||
| chr3:133421046
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+20474G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421046 | ||||||
| chr3:133421148
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+20576G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421148 | ||||||
| chr3:133421175
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(4): Show | 10 | HG01255.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+20603T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421175 | ||||||
| chr3:133421264
|
G | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0074others(10): Show | 14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20692G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421264 | ||||||
| chr3:133421348
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0183a0001c0001t0001g0207 | 3 | NA18962.hp1 NA18990.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.489+20776A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421348 | ||||||
| chr3:133421353
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0074others(10): Show | 14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20781C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421353 | ||||||
| chr3:133421354
|
A | G | 1 | a0001c0002t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+20782A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421354 | ||||||
| chr3:133421374
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 265 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.489+20802G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421374 | ||||||
| chr3:133421383
|
C | G | 1 | a0001c0002t0001g0246 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.489+20811C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421383 | ||||||
| chr3:133421383
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.489+20811C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421383 | ||||||
| chr3:133421410
|
G | A | 2 | a0001c0001t0001g0242a0001c0002t0001g0166 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+20838G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421410 | ||||||
| chr3:133421417
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+20845C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421417 | ||||||
| chr3:133421426
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.489+20854C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421426 | ||||||
| chr3:133421479
|
C | T | 16 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0083others(13): Show | 16 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+20907C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421479 | ||||||
| chr3:133421481
|
A | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0074others(10): Show | 14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20909A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421481 | ||||||
| chr3:133421497
|
A | ACTTCCTC others(2347): Show |
1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+20925_489+2092 others(2358): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421497 | ||||||
| chr3:133421501
|
T | C | 1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+20929T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421501 | ||||||
| chr3:133421658
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 181 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.489+21086G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421658 | ||||||
| chr3:133421834
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.489+21262C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421834 | ||||||
| chr3:133421886
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+21314A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421886 | ||||||
| chr3:133421920
|
T | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(33): Show | 37 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.489+21348T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421920 | ||||||
| chr3:133422000
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+21428G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422000 | ||||||
| chr3:133422063
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+21491C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422063 | ||||||
| chr3:133422076
|
C | CAGCCTGG others(6): Show |
1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+21508_489+2152 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422076 | |||||
| chr3:133422105
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.489+21554dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | |||||
| chr3:133422105
|
C | CAA | 37 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0043others(34): Show | 37 | HG00423.hp2 HG00738.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.489+21553_489+2155 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | |||||
| chr3:133422105
|
C | CAAA | 22 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 23 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.489+21552_489+2155 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | |||||
| chr3:133422105
|
C | CAAAA | 11 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+21551_489+2155 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | |||||
| chr3:133422105
|
C | CAAAAA | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+21550_489+2155 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | |||||
| chr3:133422164
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.489+21592T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422164 | ||||||
| chr3:133422375
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489+21803G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422375 | ||||||
| chr3:133422476
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.489+21904C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422476 | ||||||
| chr3:133422765
|
C | CTGCCAGA others(15): Show |
222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 227 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.489+22199_489+2222 others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422765 | |||||
| chr3:133422765
|
C | CTGCCAGA others(14): Show |
1 | a0001c0001t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.489+22209_489+2221 others(25): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422765 | |||||
| chr3:133422784
|
G | GTGTTGCC others(15): Show |
1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+22220_489+2222 others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422784 | |||||
| chr3:133422791
|
C | CAGAATAT others(16): Show |
1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+22220_489+2222 others(27): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422791 | |||||
| chr3:133422796
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(222): Show | 230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.489+22224A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422796 | ||||||
| chr3:133422803
|
T | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+22231T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422803 | ||||||
| chr3:133422830
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+22258T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422830 | ||||||
| chr3:133422853
|
C | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0110others(8): Show | 11 | HG02055.hp1 HG02165.hp1 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+22281C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422853 | ||||||
| chr3:133423270
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.489+22698G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423270 | ||||||
| chr3:133423316
|
T | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(36): Show | 40 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.489+22744T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423316 | ||||||
| chr3:133423458
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489+22886T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423458 | ||||||
| chr3:133423478
|
G | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(49): Show | 52 | HG00735.hp2 HG01106.hp2 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.489+22906G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423478 | ||||||
| chr3:133423540
|
G | T | 1 | a0001c0002t0001g0197 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+22968G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423540 | ||||||
| chr3:133423610
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+23038A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423610 | ||||||
| chr3:133423706
|
G | T | 1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+23134G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423706 | ||||||
| chr3:133423748
|
T | G | 1 | a0001c0002t0001g0197 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+23176T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423748 | ||||||
| chr3:133423749
|
G | T | 1 | a0001c0002t0001g0197 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+23177G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423749 | ||||||
| chr3:133423767
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+23195C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423767 | ||||||
| chr3:133423903
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+23331C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423903 | ||||||
| chr3:133423916
|
C | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.489+23344C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423916 | ||||||
| chr3:133424009
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.490-23308G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424009 | ||||||
| chr3:133424039
|
C | CT | 59 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 60 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.490-23267dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424039 | |||||
| chr3:133424212
|
ATTTTTTT others(5): Show |
A | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-23087_490-2307 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424212 | |||||
| chr3:133424214
|
T | TTGTGTGT others(17): Show |
1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.490-23102_490-2310 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | |||||
| chr3:133424214
|
T | TTGTGTGT others(19): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0257 | 2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.490-23102_490-2310 others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | |||||
| chr3:133424214
|
T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-23102_490-2310 others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | |||||
| chr3:133424216
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0140others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-23101T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424216 | ||||||
| chr3:133424216
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.490-23101_490-2310 others(23): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424216 | ||||||
| chr3:133424216
|
T | TTG | 16 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0060others(13): Show | 16 | HG02055.hp1 HG02165.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTG | 11 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0134others(8): Show | 11 | HG01099.hp1 HG01167.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTG | 5 | a0001c0001t0001g0069a0001c0001t0001g0157a0001c0002t0001g0062others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(9): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(21): Show |
1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(29): Show |
1 | a0001c0001t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-23100_490-2309 others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424216
|
T | TTGTGTGT others(33): Show |
1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-23100_490-2309 others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | |||||
| chr3:133424218
|
T | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(48): Show | 52 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.490-23099T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424218 | ||||||
| chr3:133424218
|
T | TTGTG | 17 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0001g0235others(14): Show | 17 | HG00438.hp1 HG00438.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-23098_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424218 | |||||
| chr3:133424220
|
T | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(66): Show | 70 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.490-23097T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424220 | ||||||
| chr3:133424220
|
T | TTGTG | 43 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(40): Show | 45 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.490-23096_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424220 | |||||
| chr3:133424220
|
T | TTGTGTG | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0204others(8): Show | 11 | HG00639.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-23096_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424220 | |||||
| chr3:133424222
|
T | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 128 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.490-23095T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424222 | ||||||
| chr3:133424222
|
T | TGTGTG | 3 | a0001c0001t0001g0219a0001c0002t0001g0120a0001c0002t0001g0213 | 3 | HG04184.hp2 NA18964.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.490-23095_490-2309 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424222 | ||||||
| chr3:133424222
|
T | TTGTG | 49 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0042others(46): Show | 50 | HG00558.hp1 HG00558.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-23094_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | |||||
| chr3:133424222
|
T | TTGTGTG | 10 | a0001c0001t0001g0051a0001c0001t0001g0195a0001c0001t0001g0198others(7): Show | 10 | NA18946.hp1 NA18946.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-23094_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | |||||
| chr3:133424222
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-23094_490-2309 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | |||||
| chr3:133424224
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-23093T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424224 | ||||||
| chr3:133424226
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 199 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.490-23091T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424226 | ||||||
| chr3:133424228
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.490-23089T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424228 | ||||||
| chr3:133424230
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.490-23087T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424230 | ||||||
| chr3:133424232
|
T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.490-23085T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424232 | ||||||
| chr3:133424234
|
T | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-23083T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424234 | ||||||
| chr3:133424236
|
T | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-23081T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424236 | ||||||
| chr3:133424238
|
T | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-23079T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424238 | ||||||
| chr3:133424240
|
T | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-23077T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424240 | ||||||
| chr3:133424244
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-23073A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424244 | ||||||
| chr3:133424244
|
A | T | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-23073A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424244 | ||||||
| chr3:133424413
|
C | CTTTTTCA others(38): Show |
1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490-22902_490-2285 others(49): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424413 | |||||
| chr3:133424474
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-22843A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424474 | ||||||
| chr3:133424511
|
TG | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-22805delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424511 | ||||||
| chr3:133424548
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-22769T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424548 | ||||||
| chr3:133424583
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-22734T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424583 | ||||||
| chr3:133424605
|
GGTTT | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0002t0001g0194 | 3 | HG00423.hp1 HG00423.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.490-22703_490-2270 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424605 | |||||
| chr3:133424625
|
T | G | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22692T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424625 | ||||||
| chr3:133424661
|
A | C | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22656A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424661 | ||||||
| chr3:133424668
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.490-22649C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424668 | ||||||
| chr3:133424669
|
T | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-22648T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424669 | ||||||
| chr3:133424786
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-22531A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424786 | ||||||
| chr3:133424812
|
T | G | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22505T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424812 | ||||||
| chr3:133424880
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.490-22437T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424880 | ||||||
| chr3:133425026
|
T | TG | 3 | a0001c0001t0001g0148a0001c0002t0001g0131a0001c0002t0001g0208 | 3 | HG02622.hp2 HG02698.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.490-22288dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425026 | |||||
| chr3:133425177
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0261 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-22140T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425177 | ||||||
| chr3:133425195
|
A | C | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-22122A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425195 | ||||||
| chr3:133425224
|
A | G | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-22093A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425224 | ||||||
| chr3:133425225
|
G | GGGGGGGG others(9): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-22092_490-2209 others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425225 | ||||||
| chr3:133425235
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-22082T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425235 | ||||||
| chr3:133425423
|
C | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-21894C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425423 | ||||||
| chr3:133425433
|
G | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0138a0002c0003t0001g0145 | 3 | HG02280.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.490-21884G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425433 | ||||||
| chr3:133425451
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-21866C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425451 | ||||||
| chr3:133425527
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21790G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425527 | ||||||
| chr3:133425539
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-21778A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425539 | ||||||
| chr3:133425611
|
A | G | 1 | a0001c0002t0001g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-21706A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425611 | ||||||
| chr3:133425644
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-21673G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425644 | ||||||
| chr3:133425762
|
G | GACGGGAA others(5): Show |
1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21554_490-2155 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425762 | |||||
| chr3:133425762
|
GATGGGA | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(13): Show | 16 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-21553_490-2154 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425762 | |||||
| chr3:133425764
|
T | A | 2 | a0001c0001t0001g0148a0006c0009t0001g0167 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.490-21553T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425764 | ||||||
| chr3:133425764
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.490-21553T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425764 | ||||||
| chr3:133425768
|
AAAGGGAA others(4): Show |
A | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-21546_490-2153 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425768 | |||||
| chr3:133425770
|
A | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(13): Show | 16 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-21547A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425770 | ||||||
| chr3:133425774
|
AAAGGGAA others(4): Show |
A | 26 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0017others(23): Show | 27 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21535_490-2152 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425774 | |||||
| chr3:133425777
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21540G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425777 | ||||||
| chr3:133425780
|
AAAGGG | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.490-21518_490-2151 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425780 | |||||
| chr3:133425784
|
G | GGAAGGGA others(6): Show |
12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21531_490-2151 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425784 | |||||
| chr3:133425785
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-21532G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425785 | ||||||
| chr3:133425785
|
G | GAAAGGGA | 3 | a0001c0001t0001g0015a0001c0001t0001g0137a0001c0001t0001g0263 | 3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21530_490-2152 others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425785 | |||||
| chr3:133425785
|
G | GAAAGGGA others(6): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0261 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21530_490-2152 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425785 | |||||
| chr3:133425787
|
A | AAG | 26 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 27 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21530_490-2152 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425787 | ||||||
| chr3:133425788
|
G | GGGAAGGG others(52): Show |
2 | a0001c0002t0001g0210a0001c0002t0001g0216 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.490-21519_490-2151 others(63): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425788 | |||||
| chr3:133425790
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(8): Show | 11 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-21527G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425790 | ||||||
| chr3:133425793
|
G | A | 1 | a0002c0003t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490-21524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425793 | ||||||
| chr3:133425800
|
GAAGAAGG others(21): Show |
G | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-21516_490-2148 others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425800 | ||||||
| chr3:133425803
|
G | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425803 | ||||||
| chr3:133425804
|
A | T | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21513A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425804 | ||||||
| chr3:133425806
|
G | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21511G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425806 | ||||||
| chr3:133425807
|
G | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21510G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425807 | ||||||
| chr3:133425807
|
G | GGAAGGGA others(11): Show |
45 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 46 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.490-21483_490-2146 others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | |||||
| chr3:133425807
|
G | GGAAGGGA others(29): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0261a0001c0001t0001g0267 | 3 | HG02109.hp2 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21501_490-2146 others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | |||||
| chr3:133425807
|
GGAAGGGA others(11): Show |
G | 2 | a0001c0002t0001g0202a0001c0002t0001g0222 | 2 | HG00735.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.490-21483_490-2146 others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | |||||
| chr3:133425825
|
A | AGAAGGGA others(16): Show |
1 | a0001c0001t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21488_490-2146 others(27): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425825 | |||||
| chr3:133425846
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-21471A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425846 | ||||||
| chr3:133425853
|
G | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-21464G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425853 | ||||||
| chr3:133425856
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490-21461A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425856 | ||||||
| chr3:133425864
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21453G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425864 | ||||||
| chr3:133425900
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21417A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425900 | ||||||
| chr3:133425913
|
G | GGGCAAGG others(3): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-21400_490-2139 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425913 | |||||
| chr3:133425943
|
A | AGGCTAGG others(85): Show |
2 | a0001c0002t0001g0039a0001c0002t0001g0203 | 2 | HG00735.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(96): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(90): Show |
11 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0074others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(79): Show |
1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.490-21372_490-2137 others(90): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(90): Show |
5 | a0001c0001t0001g0026a0001c0001t0001g0138a0001c0001t0001g0161others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(101): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0162others(4): Show | 7 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(112): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(145): Show |
1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(156): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(97): Show |
1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(108): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(80): Show |
1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21372_490-2137 others(91): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(73): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0261 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(84): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(74): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0137a0001c0001t0001g0263 | 3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(85): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(69): Show |
18 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0043others(15): Show | 18 | HG02055.hp1 HG02165.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(80): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(80): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0241others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(91): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(114): Show |
1 | a0001c0001t0001g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(125): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGCTAGG others(77): Show |
1 | a0001c0001t0001g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425943
|
A | AGGGAGGG others(435): Show |
1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-21366_490-2136 others(446): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | |||||
| chr3:133425946
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21371G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425946 | ||||||
| chr3:133425952
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-21365A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425952 | ||||||
| chr3:133425953
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 52 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.490-21364G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425953 | ||||||
| chr3:133425953
|
G | GGGGGAAG others(81): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0269 | 3 | HG02717.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(92): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(92): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG02109.hp1 HG02970.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-21359_490-2135 others(103): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(150): Show |
1 | a0001c0002t0001g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(161): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(145): Show |
2 | a0001c0001t0001g0152a0001c0002t0001g0132 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(156): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(151): Show |
1 | a0001c0002t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(184): Show |
1 | a0001c0002t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(195): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(162): Show |
3 | a0001c0001t0001g0055a0001c0001t0001g0100a0001c0002t0001g0243 | 3 | HG03669.hp1 NA18969.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(167): Show |
1 | a0001c0001t0001g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(178): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(151): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0184others(7): Show | 11 | HG01255.hp2 HG02129.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-21359_490-2135 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(167): Show |
1 | a0001c0001t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(178): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(140): Show |
1 | a0001c0008t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(151): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(152): Show |
1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(163): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(153): Show |
1 | a0001c0001t0001g0104 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(164): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(93): Show |
1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(104): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(154): Show |
1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAAG others(163): Show |
1 | a0001c0002t0001g0048 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(174): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAGG others(574): Show |
1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-21355_490-2135 others(585): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425953
|
G | GGGGGAGG others(564): Show |
1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21355_490-2135 others(575): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | |||||
| chr3:133425957
|
G | A | 2 | a0001c0001t0001g0069a0001c0002t0001g0178 | 2 | HG00738.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.490-21360G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425957 | ||||||
| chr3:133425957
|
G | GGAAGTGG others(154): Show |
1 | a0001c0002t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.490-21360_490-2135 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425957 | ||||||
| chr3:133425958
|
A | AAGTGGAG others(165): Show |
1 | a0001c0002t0001g0064 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(176): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | ||||||
| chr3:133425958
|
A | AAGTGGAG others(231): Show |
1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(242): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | ||||||
| chr3:133425958
|
A | AAGTGGAG others(152): Show |
1 | a0002c0007t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(163): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | ||||||
| chr3:133425958
|
A | AAGTGGAG others(164): Show |
1 | a0001c0002t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(175): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | ||||||
| chr3:133425958
|
A | AGTGGAGG others(148): Show |
1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-21358_490-2135 others(159): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425958 | |||||
| chr3:133425958
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.490-21359A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | ||||||
| chr3:133425959
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.490-21358G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425959 | ||||||
| chr3:133425959
|
G | GGGGAGGG others(441): Show |
1 | a0002c0003t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490-21355_490-2135 others(452): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | |||||
| chr3:133425959
|
G | GGGGAGGG others(176): Show |
1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-21355_490-2135 others(187): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | |||||
| chr3:133425959
|
G | GGGGGGAG others(511): Show |
1 | a0001c0001t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.490-21354_490-2135 others(522): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | |||||
| chr3:133425961
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.490-21356G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425961 | ||||||
| chr3:133425963
|
G | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(21): Show | 24 | HG02055.hp1 HG02165.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-21354G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425963 | ||||||
| chr3:133425964
|
A | AGGGGAGG others(503): Show |
1 | a0001c0001t0001g0183 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(514): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(505): Show |
1 | a0001c0001t0001g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(516): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(498): Show |
1 | a0001c0001t0001g0207 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(509): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(510): Show |
1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(521): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(517): Show |
1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(528): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(439): Show |
1 | a0001c0001t0001g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(450): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(406): Show |
1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(417): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(413): Show |
1 | a0001c0001t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(424): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(444): Show |
1 | a0001c0001t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(455): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(423): Show |
1 | a0001c0001t0001g0083 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(434): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(435): Show |
1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(446): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(384): Show |
1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(395): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(448): Show |
1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(459): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(418): Show |
1 | a0001c0002t0001g0211 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(429): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGAGG others(371): Show |
1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(382): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | AGGGGATG others(241): Show |
1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-21344_490-2134 others(252): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | |||||
| chr3:133425964
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-21353A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425964 | ||||||
| chr3:133425966
|
G | GGGAGGGG others(506): Show |
1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(517): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425966 | |||||
| chr3:133425968
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21349G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425968 | ||||||
| chr3:133425969
|
A | AGGGGGAG others(90): Show |
1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | ||||||
| chr3:133425969
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0068others(4): Show | 7 | HG00099.hp2 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-21348A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | ||||||
| chr3:133425969
|
AT | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(115): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.490-21347delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | ||||||
| chr3:133425969
|
ATG | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 76 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.490-21347_490-2134 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | ||||||
| chr3:133425970
|
T | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0032others(5): Show | 8 | HG00099.hp2 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-21347T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425970 | ||||||
| chr3:133425970
|
T | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(45): Show | 49 | HG00558.hp1 HG00738.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.490-21347T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425970 | ||||||
| chr3:133425971
|
G | GGGA | 23 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(20): Show | 23 | HG02055.hp1 HG02165.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.490-21344_490-2134 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(105): Show |
1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(116): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(100): Show |
9 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0027others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-21343_490-2134 others(111): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(116): Show |
1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(127): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(122): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490-21343_490-2134 others(133): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(111): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0257 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-21343_490-2134 others(122): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(151): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-21343_490-2134 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425971
|
G | GGGGAGGG others(52): Show |
1 | a0001c0001t0001g0245 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(63): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | |||||
| chr3:133425975
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-21342G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425975 | ||||||
| chr3:133425980
|
G | GAGGGGGA others(159): Show |
1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(170): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(143): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0223 | 2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(154): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(127): Show |
1 | a0001c0001t0001g0071 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(138): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(154): Show |
7 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0073others(4): Show | 7 | HG01255.hp1 HG01346.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(155): Show |
1 | a0001c0001t0001g0234 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(154): Show |
1 | a0001c0001t0001g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(84): Show |
2 | a0001c0002t0001g0111a0001c0002t0001g0233 | 2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(95): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(150): Show |
1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(161): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(159): Show |
1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(170): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(203): Show |
1 | a0001c0001t0001g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(214): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(188): Show |
1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(199): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(171): Show |
9 | a0001c0001t0001g0042a0001c0001t0001g0094a0001c0001t0001g0157others(6): Show | 9 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(182): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(172): Show |
1 | a0001c0002t0001g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(183): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(155): Show |
1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(172): Show |
1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(183): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(208): Show |
1 | a0001c0001t0001g0045 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(219): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(192): Show |
1 | a0001c0002t0001g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(203): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(160): Show |
62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(59): Show | 63 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(171): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(165): Show |
1 | a0001c0002t0001g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(176): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(181): Show |
4 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0195others(1): Show | 4 | NA18946.hp2 NA18956.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(192): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
1 | a0001c0001t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0222 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(144): Show |
1 | a0001c0002t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(155): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(149): Show |
1 | a0001c0001t0001g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(160): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(171): Show |
3 | a0001c0001t0001g0046a0001c0002t0001g0047a0001c0002t0001g0116 | 3 | NA18960.hp2 NA18983.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(182): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
2 | a0001c0002t0001g0038a0001c0002t0001g0077 | 2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(149): Show |
1 | a0001c0002t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(160): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(161): Show |
1 | a0001c0001t0001g0224 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(176): Show |
2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(187): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(166): Show |
1 | a0001c0002t0001g0248 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(177): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGG others(155): Show |
1 | a0001c0001t0001g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGG others(168): Show |
1 | a0001c0002t0001g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(179): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GAGGGGGG others(173): Show |
1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(184): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | |||||
| chr3:133425980
|
G | GGAGGGGG others(168): Show |
1 | a0001c0002t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.490-21337_490-2133 others(179): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425980 | ||||||
| chr3:133425981
|
A | G | 2 | a0001c0001t0001g0098a0001c0002t0001g0035 | 2 | HG01175.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-21336A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425981 | ||||||
| chr3:133425982
|
A | AGGGGAGG others(504): Show |
1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21333_490-2133 others(515): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425982 | |||||
| chr3:133425982
|
A | AGGGGGAG others(193): Show |
1 | a0001c0001t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.490-21333_490-2133 others(204): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425982 | |||||
| chr3:133425982
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.490-21335A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425982 | ||||||
| chr3:133425983
|
G | GGGGGAGG others(460): Show |
1 | a0001c0001t0001g0098 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.490-21333_490-2133 others(471): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425983 | |||||
| chr3:133425985
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.490-21332C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425985 | ||||||
| chr3:133425985
|
C | CAGGGCAG others(3): Show |
2 | a0001c0002t0001g0178a0001c0002t0001g0194 | 2 | HG00423.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.490-21323_490-2132 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425985 | |||||
| chr3:133425985
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21332C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425985 | ||||||
| chr3:133425987
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21330G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425987 | ||||||
| chr3:133425991
|
A | AGGGAAGG others(4): Show |
2 | a0001c0001t0001g0104a0002c0007t0001g0236 | 2 | HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.490-21323_490-2132 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425991 | |||||
| chr3:133425994
|
G | T | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-21323G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425994 | ||||||
| chr3:133425995
|
C | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0097others(24): Show | 28 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-21322C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425995 | ||||||
| chr3:133425995
|
C | G | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21322C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425995 | ||||||
| chr3:133426000
|
C | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-21317C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426000 | ||||||
| chr3:133426002
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-21315G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426002 | ||||||
| chr3:133426004
|
G | GCAGGGCA others(33): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0097others(21): Show | 25 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.490-21313_490-2131 others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | ||||||
| chr3:133426004
|
G | GCAGGGCA others(43): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | NA18964.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.490-21313_490-2131 others(54): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | ||||||
| chr3:133426004
|
G | GGCAGGGC others(36): Show |
1 | a0001c0002t0001g0064 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21313_490-2131 others(47): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | ||||||
| chr3:133426005
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21312A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426005 | ||||||
| chr3:133426007
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(47): Show | 51 | HG01123.hp2 HG01175.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.490-21310A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426007 | ||||||
| chr3:133426007
|
AGGAAG | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0199others(3): Show | 6 | HG00621.hp2 HG02015.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-21280_490-2127 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426007 | |||||
| chr3:133426014
|
G | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0097others(24): Show | 28 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-21303G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426014 | ||||||
| chr3:133426014
|
G | GAAGGAAA others(18): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-21299_490-2129 others(29): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426014 | |||||
| chr3:133426014
|
G | GAAGGGAA others(23): Show |
193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-21294_490-2129 others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426014 | |||||
| chr3:133426019
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-21298G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426019 | ||||||
| chr3:133426022
|
G | A | 1 | a0001c0002t0001g0064 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21295G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426022 | ||||||
| chr3:133426024
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 242 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.490-21293G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426024 | ||||||
| chr3:133426025
|
A | AAGGGAAA others(24): Show |
1 | a0001c0002t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-21286_490-2128 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426025 | |||||
| chr3:133426026
|
A | AGGAAAGA others(23): Show |
1 | a0001c0002t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.490-21289_490-2128 others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426026 | |||||
| chr3:133426026
|
A | AGGGAAAG others(24): Show |
1 | a0001c0001t0001g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-21286_490-2128 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426026 | |||||
| chr3:133426032
|
G | A | 1 | a0001c0002t0001g0064 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21285G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426032 | ||||||
| chr3:133426055
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21262G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426055 | ||||||
| chr3:133426095
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21222C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426095 | ||||||
| chr3:133426102
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21215C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426102 | ||||||
| chr3:133426103
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21214A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426103 | ||||||
| chr3:133426184
|
C | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0138a0002c0003t0001g0145 | 3 | HG02280.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.490-21133C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426184 | ||||||
| chr3:133426298
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0137a0001c0001t0001g0263 | 3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21019G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426298 | ||||||
| chr3:133426308
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-21009A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426308 | ||||||
| chr3:133426436
|
A | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.490-20881A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426436 | ||||||
| chr3:133426451
|
A | G | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-20866A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426451 | ||||||
| chr3:133426486
|
G | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 35 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.490-20831G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426486 | ||||||
| chr3:133426615
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.490-20702G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426615 | ||||||
| chr3:133426624
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-20693T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426624 | ||||||
| chr3:133426625
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-20692C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426625 | ||||||
| chr3:133426646
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.490-20671C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426646 | ||||||
| chr3:133426727
|
T | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-20590T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426727 | ||||||
| chr3:133426743
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 238 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.490-20574A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426743 | ||||||
| chr3:133426762
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-20555G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426762 | ||||||
| chr3:133426911
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-20406T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426911 | ||||||
| chr3:133426926
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-20391G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426926 | ||||||
| chr3:133426945
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490-20372T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426945 | ||||||
| chr3:133427028
|
C | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01243.hp2 HG03471.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-20289C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427028 | ||||||
| chr3:133427117
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.490-20200C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427117 | ||||||
| chr3:133427379
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 266 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.490-19938G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427379 | ||||||
| chr3:133427403
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490-19914G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427403 | ||||||
| chr3:133427514
|
T | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-19803T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427514 | ||||||
| chr3:133427517
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-19800A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427517 | ||||||
| chr3:133427578
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-19739C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427578 | ||||||
| chr3:133427585
|
C | A | 1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-19732C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427585 | ||||||
| chr3:133427683
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.490-19634C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427683 | ||||||
| chr3:133427696
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-19621T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427696 | ||||||
| chr3:133427705
|
C | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-19612C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427705 | ||||||
| chr3:133427818
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490-19499A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427818 | ||||||
| chr3:133427941
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-19376A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427941 | ||||||
| chr3:133428016
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-19301A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428016 | ||||||
| chr3:133428061
|
T | C | 1 | a0001c0002t0002g0214 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.490-19256T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428061 | ||||||
| chr3:133428226
|
C | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-19091C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428226 | ||||||
| chr3:133428240
|
G | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-19077G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428240 | ||||||
| chr3:133428257
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-19060C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428257 | ||||||
| chr3:133428277
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(16): Show | 20 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-19040G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428277 | ||||||
| chr3:133428282
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-19035A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428282 | ||||||
| chr3:133428289
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-19028A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428289 | ||||||
| chr3:133428331
|
G | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-18986G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428331 | ||||||
| chr3:133428334
|
AG | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18980delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428334 | |||||
| chr3:133428339
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-18978G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428339 | ||||||
| chr3:133428384
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-18933A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428384 | ||||||
| chr3:133428431
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-18886A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428431 | ||||||
| chr3:133428482
|
C | CA | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.490-18824dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428482 | |||||
| chr3:133428498
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-18819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428498 | ||||||
| chr3:133428592
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-18725G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428592 | ||||||
| chr3:133428657
|
GA | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-18657delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428657 | |||||
| chr3:133428673
|
T | A | 1 | a0001c0002t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.490-18644T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428673 | ||||||
| chr3:133428769
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0023 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-18548C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428769 | ||||||
| chr3:133428796
|
C | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 251 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.490-18521C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428796 | ||||||
| chr3:133428803
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428803 | ||||||
| chr3:133428805
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.490-18512C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428805 | ||||||
| chr3:133428824
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-18493C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428824 | ||||||
| chr3:133428825
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18492C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428825 | ||||||
| chr3:133428875
|
C | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0089a0001c0002t0001g0209 | 3 | NA18952.hp2 NA19063.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.490-18442C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428875 | ||||||
| chr3:133428876
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.490-18441C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428876 | ||||||
| chr3:133428945
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-18372C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428945 | ||||||
| chr3:133429022
|
T | TA | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.490-18289dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429022 | |||||
| chr3:133429030
|
C | T | 2 | a0001c0001t0001g0014a0001c0002t0001g0172 | 2 | HG01517.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-18287C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429030 | ||||||
| chr3:133429110
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-18207C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429110 | ||||||
| chr3:133429111
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-18206A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429111 | ||||||
| chr3:133429116
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.490-18201C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429116 | ||||||
| chr3:133429118
|
C | G | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-18199C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429118 | ||||||
| chr3:133429136
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-18181T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429136 | ||||||
| chr3:133429286
|
T | G | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-18031T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429286 | ||||||
| chr3:133429326
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0137a0001c0001t0001g0263 | 3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-17991G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429326 | ||||||
| chr3:133429379
|
T | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17938T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429379 | ||||||
| chr3:133429391
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17926A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429391 | ||||||
| chr3:133429498
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 62 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.490-17819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429498 | ||||||
| chr3:133429507
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.490-17810C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429507 | ||||||
| chr3:133429574
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17743G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429574 | ||||||
| chr3:133429659
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17658G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429659 | ||||||
| chr3:133429765
|
T | TA | 35 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(32): Show | 36 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.490-17552_490-1755 others(5): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429765 | ||||||
| chr3:133429765
|
T | TTA | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.490-17551_490-1755 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429765 | |||||
| chr3:133429774
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.490-17543C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429774 | ||||||
| chr3:133429803
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429803 | ||||||
| chr3:133429828
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-17489A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429828 | ||||||
| chr3:133429838
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.490-17479T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429838 | ||||||
| chr3:133429897
|
C | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-17420C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429897 | ||||||
| chr3:133429904
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.490-17413A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429904 | ||||||
| chr3:133429907
|
A | AC | 21 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0041others(18): Show | 21 | HG00738.hp1 HG01106.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-17405dupC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429907 | |||||
| chr3:133429907
|
A | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17410A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429907 | ||||||
| chr3:133429920
|
A | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17397A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429920 | ||||||
| chr3:133429925
|
T | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17392T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429925 | ||||||
| chr3:133429929
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17388C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429929 | ||||||
| chr3:133429934
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-17383C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429934 | ||||||
| chr3:133429947
|
T | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17370T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429947 | ||||||
| chr3:133429959
|
T | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17358T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429959 | ||||||
| chr3:133429964
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17353T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429964 | ||||||
| chr3:133429967
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-17350C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429967 | ||||||
| chr3:133429976
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17341A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429976 | ||||||
| chr3:133430001
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17316C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430001 | ||||||
| chr3:133430010
|
G | C | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-17307G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430010 | ||||||
| chr3:133430015
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17302T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430015 | ||||||
| chr3:133430024
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(239): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.490-17293T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430024 | ||||||
| chr3:133430025
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17292G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430025 | ||||||
| chr3:133430027
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-17290T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430027 | ||||||
| chr3:133430063
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-17254T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430063 | ||||||
| chr3:133430114
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-17203C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430114 | ||||||
| chr3:133430192
|
T | G | 2 | a0001c0002t0001g0038a0001c0002t0001g0077 | 2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.490-17125T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430192 | ||||||
| chr3:133430236
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0137 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-17081A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430236 | ||||||
| chr3:133430250
|
T | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-17067T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430250 | ||||||
| chr3:133430291
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-17026A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430291 | ||||||
| chr3:133430292
|
A | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-17025A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430292 | ||||||
| chr3:133430315
|
C | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-17002C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430315 | ||||||
| chr3:133430345
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-16972C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430345 | ||||||
| chr3:133430391
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-16926A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430391 | ||||||
| chr3:133430517
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.490-16800G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430517 | ||||||
| chr3:133430533
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.490-16784T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430533 | ||||||
| chr3:133430565
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-16752G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430565 | ||||||
| chr3:133430626
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-16691G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430626 | ||||||
| chr3:133430634
|
G | A | 2 | a0001c0001t0001g0228a0002c0003t0001g0115 | 2 | HG02071.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.490-16683G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430634 | ||||||
| chr3:133430642
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.490-16675C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430642 | ||||||
| chr3:133430691
|
A | G | 15 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0072others(12): Show | 15 | HG01081.hp1 HG01255.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-16626A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430691 | ||||||
| chr3:133430692
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.490-16625T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430692 | ||||||
| chr3:133430694
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-16623C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430694 | ||||||
| chr3:133430695
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 226 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.490-16622A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430695 | ||||||
| chr3:133430761
|
G | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG01243.hp2 HG02622.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-16556G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430761 | ||||||
| chr3:133430793
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.490-16524A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430793 | ||||||
| chr3:133430837
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG01070.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-16480C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430837 | ||||||
| chr3:133430841
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.490-16476C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430841 | ||||||
| chr3:133430862
|
C | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0257 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-16455C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430862 | ||||||
| chr3:133430873
|
C | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(13): Show | 17 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-16444C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430873 | ||||||
| chr3:133430884
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-16433T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430884 | ||||||
| chr3:133430939
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-16378C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430939 | ||||||
| chr3:133431063
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0104 | 2 | HG01993.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.490-16254C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431063 | ||||||
| chr3:133431067
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.490-16250G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431067 | ||||||
| chr3:133431077
|
TGGTTCGT others(2): Show |
T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.490-16237_490-1622 others(13): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133431077 | |||||
| chr3:133431104
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(23): Show | 26 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-16213G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431104 | ||||||
| chr3:133431140
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(23): Show | 26 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-16177G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431140 | ||||||
| chr3:133431347
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-15970A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431347 | ||||||
| chr3:133431394
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.490-15923G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431394 | ||||||
| chr3:133431442
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 243 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.490-15875C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431442 | ||||||
| chr3:133431484
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-15833G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431484 | ||||||
| chr3:133431535
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.490-15782C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431535 | ||||||
| chr3:133431607
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15710G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431607 | ||||||
| chr3:133431611
|
G | A | 119 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0050others(116): Show | 119 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.490-15706G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431611 | ||||||
| chr3:133431643
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 40 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-15674C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431643 | ||||||
| chr3:133431666
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 238 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.490-15651C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431666 | ||||||
| chr3:133431677
|
T | C | 2 | a0001c0001t0001g0106a0001c0002t0001g0035 | 2 | HG03239.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-15640T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431677 | ||||||
| chr3:133431680
|
A | G | 2 | a0001c0001t0001g0106a0001c0002t0001g0035 | 2 | HG03239.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-15637A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431680 | ||||||
| chr3:133431698
|
C | CG | 4 | a0001c0001t0001g0148a0001c0001t0001g0267a0001c0002t0001g0056others(1): Show | 4 | HG02109.hp2 HG02622.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-15618dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133431698 | |||||
| chr3:133431698
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490-15619C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431698 | ||||||
| chr3:133431712
|
C | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-15605C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431712 | ||||||
| chr3:133431735
|
T | C | 20 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(17): Show | 20 | HG00738.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-15582T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431735 | ||||||
| chr3:133431738
|
A | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(16): Show | 19 | HG00738.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-15579A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431738 | ||||||
| chr3:133431777
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(8): Show | 12 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-15540C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431777 | ||||||
| chr3:133431806
|
A | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0022others(20): Show | 23 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.490-15511A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431806 | ||||||
| chr3:133431831
|
C | T | 70 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(67): Show | 70 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.490-15486C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431831 | ||||||
| chr3:133431845
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15472C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431845 | ||||||
| chr3:133431869
|
C | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-15448C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431869 | ||||||
| chr3:133431978
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-15339G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431978 | ||||||
| chr3:133431989
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.490-15328A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431989 | ||||||
| chr3:133431998
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15319C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431998 | ||||||
| chr3:133432010
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-15307C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432010 | ||||||
| chr3:133432019
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-15298A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432019 | ||||||
| chr3:133432021
|
C | CATCT | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-15295_490-1529 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133432021 | |||||
| chr3:133432094
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 242 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.490-15223T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432094 | ||||||
| chr3:133432097
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0025 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-15220C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432097 | ||||||
| chr3:133432100
|
C | T | 11 | a0001c0001t0001g0032a0001c0001t0001g0161a0001c0001t0001g0162others(8): Show | 11 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-15217C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432100 | ||||||
| chr3:133432124
|
G | A | 17 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0072others(14): Show | 17 | HG01081.hp1 HG01255.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-15193G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432124 | ||||||
| chr3:133432259
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-15058C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432259 | ||||||
| chr3:133432307
|
C | A | 2 | a0001c0002t0001g0054a0001c0002t0001g0096 | 2 | NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.490-15010C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432307 | ||||||
| chr3:133432574
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-14743A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432574 | ||||||
| chr3:133432821
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-14496G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432821 | ||||||
| chr3:133432833
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0241others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-14484C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432833 | ||||||
| chr3:133432834
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-14483G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432834 | ||||||
| chr3:133432867
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14450T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432867 | ||||||
| chr3:133432869
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14448C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432869 | ||||||
| chr3:133432872
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14445C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432872 | ||||||
| chr3:133432926
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-14391C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432926 | ||||||
| chr3:133432955
|
C | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(32): Show | 35 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-14362C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432955 | ||||||
| chr3:133433051
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0117others(1): Show | 4 | HG01993.hp1 HG02273.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-14266A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433051 | ||||||
| chr3:133433221
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-14096A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433221 | ||||||
| chr3:133433266
|
T | C | 1 | a0001c0002t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.490-14051T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433266 | ||||||
| chr3:133433412
|
C | A | 1 | a0001c0002t0001g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-13905C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433412 | ||||||
| chr3:133433421
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-13896G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433421 | ||||||
| chr3:133433433
|
A | C | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-13884A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433433 | ||||||
| chr3:133433450
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13867C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433450 | ||||||
| chr3:133433455
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13862T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433455 | ||||||
| chr3:133433456
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13861C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433456 | ||||||
| chr3:133433461
|
T | C | 2 | a0001c0002t0001g0171a0001c0002t0001g0270 | 2 | HG01167.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.490-13856T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433461 | ||||||
| chr3:133433469
|
A | G | 2 | a0001c0002t0001g0035a0001c0002t0001g0044 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-13848A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433469 | ||||||
| chr3:133433707
|
C | G | 2 | a0001c0002t0001g0035a0001c0002t0001g0044 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-13610C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433707 | ||||||
| chr3:133433775
|
C | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0083others(21): Show | 24 | HG00621.hp2 HG01175.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.490-13542C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433775 | ||||||
| chr3:133433871
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0002t0001g0180others(2): Show | 5 | HG00423.hp2 HG00597.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-13446G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433871 | ||||||
| chr3:133434026
|
A | G | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 130 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.490-13291A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434026 | ||||||
| chr3:133434197
|
A | G | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(101): Show | 105 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.490-13120A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434197 | ||||||
| chr3:133434237
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(32): Show | 35 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-13080C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434237 | ||||||
| chr3:133434278
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-13039G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434278 | ||||||
| chr3:133434328
|
T | A | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(101): Show | 105 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.490-12989T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434328 | ||||||
| chr3:133434347
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(79): Show | 83 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.490-12970T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434347 | ||||||
| chr3:133434437
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(9): Show | 12 | HG00738.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-12880G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434437 | ||||||
| chr3:133434523
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.490-12794A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434523 | ||||||
| chr3:133434646
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-12671C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434646 | ||||||
| chr3:133434647
|
A | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(61): Show | 64 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.490-12670A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434647 | ||||||
| chr3:133434706
|
T | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(19): Show | 22 | HG00738.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-12611T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434706 | ||||||
| chr3:133434760
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-12557T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434760 | ||||||
| chr3:133434761
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-12556A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434761 | ||||||
| chr3:133435325
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-11992A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435325 | ||||||
| chr3:133435331
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-11986C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435331 | ||||||
| chr3:133435410
|
C | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 41 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-11907C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435410 | ||||||
| chr3:133435612
|
C | G | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-11705C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435612 | ||||||
| chr3:133435755
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0069others(1): Show | 4 | HG00738.hp1 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-11562T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435755 | ||||||
| chr3:133435807
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.490-11510A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435807 | ||||||
| chr3:133435914
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-11403G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435914 | ||||||
| chr3:133436048
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.490-11269G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436048 | ||||||
| chr3:133436062
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.490-11255G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436062 | ||||||
| chr3:133436130
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(34): Show | 38 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.490-11187G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436130 | ||||||
| chr3:133436292
|
C | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(37): Show | 40 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-11025C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436292 | ||||||
| chr3:133436325
|
C | CA | 35 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0017others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.490-10971dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | |||||
| chr3:133436325
|
C | CAA | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0026others(33): Show | 36 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.490-10972_490-1097 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | |||||
| chr3:133436325
|
C | CAAA | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(25): Show | 29 | HG00558.hp2 HG00621.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-10973_490-1097 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | |||||
| chr3:133436325
|
C | CAAAA | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0042others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-10974_490-1097 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | |||||
| chr3:133436325
|
C | CAAAAA | 9 | a0001c0001t0001g0032a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-10975_490-1097 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | |||||
| chr3:133436348
|
C | A | 1 | a0001c0002t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490-10969C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436348 | ||||||
| chr3:133436465
|
T | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0104others(4): Show | 7 | HG01993.hp1 HG02273.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-10852T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436465 | ||||||
| chr3:133436477
|
G | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(9): Show | 12 | HG00738.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-10840G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436477 | ||||||
| chr3:133436664
|
G | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(10): Show | 13 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-10653G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436664 | ||||||
| chr3:133436704
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-10613C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436704 | ||||||
| chr3:133436754
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 28 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.490-10563G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436754 | ||||||
| chr3:133436754
|
G | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(10): Show | 13 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-10563G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436754 | ||||||
| chr3:133436765
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.490-10552C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436765 | ||||||
| chr3:133436829
|
A | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.490-10488A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436829 | ||||||
| chr3:133436924
|
AG | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(37): Show | 40 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-10391delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436924 | |||||
| chr3:133437472
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-9845G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437472 | ||||||
| chr3:133437479
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(9): Show | 12 | HG01884.hp1 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-9838C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437479 | ||||||
| chr3:133437545
|
A | G | 2 | a0001c0002t0001g0035a0001c0002t0001g0044 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-9772A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437545 | ||||||
| chr3:133437629
|
AAAAG | A | 22 | a0001c0001t0001g0061a0001c0001t0001g0083a0001c0001t0001g0098others(19): Show | 22 | HG00621.hp2 HG01099.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-9681_490-9678d others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133437629 | |||||
| chr3:133437664
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-9638_490-9629d others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133437664 | |||||
| chr3:133437770
|
C | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0023others(18): Show | 21 | HG00738.hp1 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-9547C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437770 | ||||||
| chr3:133437848
|
C | T | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(98): Show | 102 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.490-9469C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437848 | ||||||
| chr3:133437853
|
C | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0149others(1): Show | 4 | HG02451.hp1 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-9464C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437853 | ||||||
| chr3:133438082
|
T | C | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.490-9235T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438082 | ||||||
| chr3:133438262
|
C | T | 34 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(31): Show | 34 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-9055C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438262 | ||||||
| chr3:133438324
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.490-8993C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438324 | ||||||
| chr3:133438398
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-8919G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438398 | ||||||
| chr3:133438481
|
G | A | 1 | a0001c0002t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.490-8836G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438481 | ||||||
| chr3:133438492
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-8825A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438492 | ||||||
| chr3:133438497
|
T | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 29 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.490-8820T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438497 | ||||||
| chr3:133438502
|
T | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(62): Show | 66 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.490-8815T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438502 | ||||||
| chr3:133438589
|
C | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0012others(65): Show | 69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.490-8728C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438589 | ||||||
| chr3:133438722
|
T | C | 20 | a0001c0001t0001g0061a0001c0001t0001g0083a0001c0001t0001g0098others(17): Show | 20 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-8595T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438722 | ||||||
| chr3:133438778
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.490-8539C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438778 | ||||||
| chr3:133438849
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490-8468G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438849 | ||||||
| chr3:133438857
|
G | C | 2 | a0001c0002t0001g0088a0001c0002t0001g0203 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.490-8460G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438857 | ||||||
| chr3:133439142
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-8175T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439142 | ||||||
| chr3:133439200
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490-8117T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439200 | ||||||
| chr3:133439493
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.490-7824T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439493 | ||||||
| chr3:133439520
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0239others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-7797A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439520 | ||||||
| chr3:133439578
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-7739G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439578 | ||||||
| chr3:133439664
|
G | A | 95 | a0001c0001t0001g0051a0001c0001t0001g0100a0001c0001t0001g0101others(92): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.490-7653G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439664 | ||||||
| chr3:133439815
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-7502C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439815 | ||||||
| chr3:133439816
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-7501G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439816 | ||||||
| chr3:133439825
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-7492C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439825 | ||||||
| chr3:133439838
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.490-7479A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439838 | ||||||
| chr3:133439928
|
C | CAG | 26 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(23): Show | 27 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-7373_490-7372d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133439928 | |||||
| chr3:133439928
|
C | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-7389C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439928 | ||||||
| chr3:133439932
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0036others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-7385G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439932 | ||||||
| chr3:133439989
|
G | A | 130 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(127): Show | 131 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.490-7328G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439989 | ||||||
| chr3:133439990
|
T | G | 1 | a0001c0002t0001g0064 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-7327T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439990 | ||||||
| chr3:133440048
|
T | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0015others(24): Show | 27 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-7269T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440048 | ||||||
| chr3:133440197
|
C | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0259 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.490-7120C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440197 | ||||||
| chr3:133440211
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-7106G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440211 | ||||||
| chr3:133440226
|
CATGATTC others(1): Show |
C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.490-7080_490-7073d others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133440226 | |||||
| chr3:133440384
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.490-6933T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440384 | ||||||
| chr3:133440661
|
A | G | 3 | a0002c0003t0001g0003a0002c0003t0001g0154a0002c0003t0001g0252 | 4 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-6656A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440661 | ||||||
| chr3:133440754
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-6563C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440754 | ||||||
| chr3:133440873
|
G | A | 2 | a0001c0002t0001g0028a0001c0002t0001g0053 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.490-6444G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440873 | ||||||
| chr3:133441039
|
C | CT | 28 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0050others(25): Show | 28 | HG00735.hp1 HG01175.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-6259dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | |||||
| chr3:133441039
|
C | CTT | 26 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0015others(23): Show | 26 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-6260_490-6259d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | |||||
| chr3:133441039
|
CT | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(15): Show | 18 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-6259delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | |||||
| chr3:133441250
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.490-6067G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441250 | ||||||
| chr3:133441696
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-5621G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441696 | ||||||
| chr3:133441750
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-5567G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441750 | ||||||
| chr3:133441803
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.490-5514A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441803 | ||||||
| chr3:133441809
|
C | T | 4 | a0001c0002t0001g0037a0001c0002t0001g0088a0001c0002t0001g0203others(1): Show | 4 | HG00735.hp2 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5508C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441809 | ||||||
| chr3:133442033
|
A | G | 1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-5284A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442033 | ||||||
| chr3:133442067
|
G | C | 150 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0014others(147): Show | 151 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.490-5250G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442067 | ||||||
| chr3:133442353
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-4964C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442353 | ||||||
| chr3:133442385
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-4932G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442385 | ||||||
| chr3:133442449
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0143others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4868C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442449 | ||||||
| chr3:133442611
|
T | C | 1 | a0002c0003t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.490-4706T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442611 | ||||||
| chr3:133442627
|
G | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(63): Show | 66 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.490-4690G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442627 | ||||||
| chr3:133442839
|
T | G | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-4478T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442839 | ||||||
| chr3:133442862
|
C | CT | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(2): Show | 5 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-4441dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133442862 | |||||
| chr3:133442862
|
CT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-4441delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133442862 | |||||
| chr3:133442920
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0166 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.490-4397C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442920 | ||||||
| chr3:133443005
|
G | A | 19 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0071others(16): Show | 19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4312G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443005 | ||||||
| chr3:133443079
|
G | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.490-4238G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443079 | ||||||
| chr3:133443289
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-4028T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443289 | ||||||
| chr3:133443295
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(30): Show | 34 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.490-4022T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443295 | ||||||
| chr3:133443387
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 71 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.490-3930T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443387 | ||||||
| chr3:133443476
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.490-3841G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443476 | ||||||
| chr3:133443576
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-3741G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443576 | ||||||
| chr3:133443590
|
G | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0065others(15): Show | 19 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-3727G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443590 | ||||||
| chr3:133444070
|
A | G | 14 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-3247A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444070 | ||||||
| chr3:133444284
|
G | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG01081.hp1 HG01346.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3033G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444284 | ||||||
| chr3:133444480
|
A | G | 19 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0071others(16): Show | 19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-2837A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444480 | ||||||
| chr3:133444498
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.490-2819C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444498 | ||||||
| chr3:133444556
|
G | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2761G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444556 | ||||||
| chr3:133444647
|
C | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0075others(13): Show | 16 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-2670C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444647 | ||||||
| chr3:133444777
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.490-2540G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444777 | ||||||
| chr3:133444781
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-2536G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444781 | ||||||
| chr3:133444793
|
A | G | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-2524A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444793 | ||||||
| chr3:133444823
|
C | T | 2 | a0001c0002t0001g0091a0001c0002t0001g0213 | 2 | NA18972.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.490-2494C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444823 | ||||||
| chr3:133444913
|
C | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2404C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444913 | ||||||
| chr3:133444960
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0147others(1): Show | 5 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2357A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444960 | ||||||
| chr3:133445008
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.490-2309G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445008 | ||||||
| chr3:133445018
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0029others(21): Show | 24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-2299A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445018 | ||||||
| chr3:133445047
|
G | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2270G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445047 | ||||||
| chr3:133445169
|
T | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(31): Show | 34 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-2148T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445169 | ||||||
| chr3:133445397
|
G | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0029others(21): Show | 24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1920G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445397 | ||||||
| chr3:133445884
|
AG | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-1430delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133445884 | |||||
| chr3:133445944
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-1373C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445944 | ||||||
| chr3:133445994
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-1323G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445994 | ||||||
| chr3:133446044
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0029others(21): Show | 24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1273A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446044 | ||||||
| chr3:133446052
|
C | T | 1 | a0001c0002t0001g0266 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.490-1265C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446052 | ||||||
| chr3:133446054
|
C | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0249 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.490-1263C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446054 | ||||||
| chr3:133446106
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0137 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-1211A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446106 | ||||||
| chr3:133446335
|
A | G | 1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-982A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446335 | ||||||
| chr3:133446410
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-907G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446410 | ||||||
| chr3:133446570
|
T | A | 1 | a0001c0002t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.490-747T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446570 | ||||||
| chr3:133446570
|
T | TTA | 9 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0217others(6): Show | 9 | HG01255.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-678_490-677dup others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTATA | 4 | a0001c0001t0001g0160a0001c0001t0001g0181a0001c0001t0001g0228others(1): Show | 4 | HG01192.hp2 HG02055.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-680_490-677dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0177a0001c0001t0001g0207 | 3 | HG03139.hp2 NA18948.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.490-684_490-677dup others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0245 | 2 | NA18956.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.490-686_490-677dup others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-690_490-677dup others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0163 | 2 | HG02145.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.490-694_490-677dup others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTTTA | 4 | a0001c0001t0001g0265a0001c0002t0001g0078a0001c0002t0001g0107others(1): Show | 4 | HG01515.hp2 NA18955.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-746_490-745ins others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTTTATA | 3 | a0001c0002t0001g0111a0001c0002t0001g0205a0002c0003t0001g0003 | 4 | HG01069.hp2 HG01071.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-746_490-745ins others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTTTATAT others(3): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-746_490-745ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
T | TTTTATAT others(5): Show |
1 | a0001c0001t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.490-746_490-745ins others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTA | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0149others(8): Show | 11 | HG01106.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-678_490-677del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATA | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0098others(13): Show | 16 | HG01070.hp2 HG01175.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-680_490-677del others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATA | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0068others(10): Show | 13 | HG00099.hp2 HG01123.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-682_490-677del others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(1): Show |
T | 22 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0043others(19): Show | 22 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-684_490-677del others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(3): Show |
T | 15 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0071others(12): Show | 15 | HG01106.hp2 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-686_490-677del others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0198others(5): Show | 8 | HG03041.hp2 HG03704.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-688_490-677del others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(7): Show |
T | 21 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0045others(18): Show | 21 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-690_490-677del others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(9): Show |
T | 18 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG00423.hp1 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-692_490-677del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(11): Show |
T | 15 | a0001c0001t0001g0021a0001c0001t0001g0065a0001c0001t0001g0069others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-694_490-677del others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(13): Show |
T | 11 | a0001c0001t0001g0093a0001c0001t0001g0185a0001c0002t0001g0037others(8): Show | 11 | HG02083.hp1 HG02523.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-696_490-677del others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(15): Show |
T | 13 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0002t0001g0054others(10): Show | 13 | HG01891.hp1 HG02015.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-698_490-677del others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.490-700_490-677del others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0083 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.490-702_490-677del others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(21): Show |
T | 4 | a0001c0001t0001g0106a0001c0001t0001g0147a0001c0001t0001g0169others(1): Show | 4 | HG01884.hp2 HG03017.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-704_490-677del others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490-706_490-677del others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(25): Show |
T | 2 | a0001c0001t0001g0002a0001c0001t0001g0023 | 3 | HG02257.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490-708_490-677del others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(27): Show |
T | 2 | a0001c0001t0001g0138a0001c0001t0001g0271 | 2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.490-710_490-677del others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(29): Show |
T | 1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-712_490-677del others(36): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(31): Show |
T | 5 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0257others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-714_490-677del others(38): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(33): Show |
T | 6 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0002t0001g0067others(3): Show | 8 | HG00735.hp2 HG01255.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-716_490-677del others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(35): Show |
T | 6 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG01243.hp2 HG01257.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-718_490-677del others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(37): Show |
T | 3 | a0001c0001t0001g0015a0001c0001t0001g0137a0005c0006t0001g0264 | 3 | HG02257.hp1 HG04204.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-720_490-677del others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(43): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.490-726_490-677del others(50): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446570
|
TTATATAT others(51): Show |
T | 10 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0024others(7): Show | 10 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-734_490-677del others(58): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | |||||
| chr3:133446571
|
TATATATA others(4): Show |
T | 2 | a0001c0002t0001g0227a0003c0010t0001g0156 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.490-745_490-735del others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | ||||||
| chr3:133446571
|
TATATATA others(8): Show |
T | 1 | a0001c0002t0001g0048 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.490-745_490-731del others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | ||||||
| chr3:133446571
|
TATATATA others(10): Show |
T | 2 | a0001c0001t0001g0229a0001c0002t0002g0214 | 2 | HG02004.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.490-745_490-729del others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | ||||||
| chr3:133446572
|
A | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0144a0001c0001t0001g0179others(5): Show | 8 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-745A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446572 | ||||||
| chr3:133446574
|
A | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0149others(6): Show | 9 | HG01516.hp1 HG01517.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-743A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446574 | ||||||
| chr3:133446576
|
A | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0148a0001c0001t0001g0249others(5): Show | 8 | HG01070.hp2 HG01928.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-741A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446576 | ||||||
| chr3:133446578
|
A | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0097a0001c0001t0001g0176others(2): Show | 5 | HG00099.hp2 HG02886.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-739A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446578 | ||||||
| chr3:133446579
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-738T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446579 | ||||||
| chr3:133446580
|
A | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0079a0001c0001t0001g0081others(13): Show | 16 | HG01952.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-737A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446580 | ||||||
| chr3:133446581
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-736T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446581 | ||||||
| chr3:133446582
|
A | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0112a0001c0001t0001g0113others(6): Show | 9 | HG01106.hp2 HG01123.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-735A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446582 | ||||||
| chr3:133446583
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.490-734T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446583 | ||||||
| chr3:133446584
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0198others(5): Show | 8 | HG03041.hp2 HG03704.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-733A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446584 | ||||||
| chr3:133446586
|
A | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0045others(16): Show | 19 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-731A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446586 | ||||||
| chr3:133446588
|
A | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00423.hp1 HG00738.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-729A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446588 | ||||||
| chr3:133446590
|
A | T | 13 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0072others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-727A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446590 | ||||||
| chr3:133446592
|
A | T | 11 | a0001c0001t0001g0093a0001c0001t0001g0185a0001c0002t0001g0037others(8): Show | 11 | HG02083.hp1 HG02523.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-725A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446592 | ||||||
| chr3:133446594
|
A | T | 8 | a0001c0001t0001g0020a0001c0002t0001g0066a0001c0002t0001g0095others(5): Show | 8 | HG01891.hp1 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-723A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446594 | ||||||
| chr3:133446596
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.490-721A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446596 | ||||||
| chr3:133446600
|
A | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0169 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.490-717A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446600 | ||||||
| chr3:133446606
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-711A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446606 | ||||||
| chr3:133446608
|
A | T | 1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-709A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446608 | ||||||
| chr3:133446610
|
A | T | 2 | a0001c0002t0001g0039a0001c0002t0001g0084 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.490-707A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446610 | ||||||
| chr3:133446612
|
A | T | 3 | a0001c0002t0001g0067a0001c0002t0001g0088a0001c0002t0001g0203 | 3 | HG00735.hp2 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.490-705A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446612 | ||||||
| chr3:133446614
|
A | T | 1 | a0001c0002t0001g0058 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.490-703A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446614 | ||||||
| chr3:133446616
|
A | T | 1 | a0005c0006t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.490-701A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446616 | ||||||
| chr3:133446625
|
TATATATA others(8): Show |
T | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-690_490-676del others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446625 | |||||
| chr3:133446639
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-678T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446639 | ||||||
| chr3:133446641
|
A | T | 1 | a0001c0002t0001g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.490-676A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446641 | ||||||
| chr3:133446642
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-675A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446642 | ||||||
| chr3:133446654
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | NA18956.hp2 NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.490-663G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446654 | ||||||
| chr3:133447017
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-300A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133447017 | ||||||
| chr3:133447559
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.572+160A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447559 | ||||||
| chr3:133447740
|
T | G | 162 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.572+341T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447740 | ||||||
| chr3:133447981
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0098 | 3 | HG01175.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.573-508G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447981 | ||||||
| chr3:133448014
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0143others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-475G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448014 | ||||||
| chr3:133448267
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0166 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.573-222T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448267 | ||||||
| chr3:133448272
|
C | T | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0116 | 3 | NA18960.hp2 NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.573-217C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448272 | ||||||
| chr3:133448273
|
G | A | 36 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.573-216G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448273 | ||||||
| chr3:133448937
|
C | T | 1 | a0002c0003t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.729+292C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133448937 | ||||||
| chr3:133448962
|
G | GT | 37 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(34): Show | 38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.729+326dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133448962 | |||||
| chr3:133449064
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0133others(2): Show | 5 | HG01884.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+419G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449064 | ||||||
| chr3:133449171
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0143others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+526G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449171 | ||||||
| chr3:133449384
|
G | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.729+739G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449384 | ||||||
| chr3:133449405
|
C | CTTTGTT | 34 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 34 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.729+781_729+786dup others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449405 | |||||
| chr3:133449468
|
T | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0240 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.729+823T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449468 | ||||||
| chr3:133449500
|
T | TTTTG | 4 | a0001c0001t0001g0069a0001c0001t0001g0135a0001c0001t0001g0149others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-771_730-768dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449500 | |||||
| chr3:133449500
|
TTTTGTTT others(1): Show |
T | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 226 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.730-775_730-768del others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449500 | |||||
| chr3:133449725
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(74): Show | 78 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.730-578A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449725 | ||||||
| chr3:133449753
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-550C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449753 | ||||||
| chr3:133449861
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0241 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.730-442C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449861 | ||||||
| chr3:133449880
|
C | A | 1 | a0001c0002t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.730-423C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449880 | ||||||
| chr3:133449949
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-354A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449949 | ||||||
| chr3:133449949
|
AAGAGAG | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0026others(20): Show | 23 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.730-348_730-343del others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449949 | |||||
| chr3:133449955
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0013others(52): Show | 56 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.730-348G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449955 | ||||||
| chr3:133449955
|
G | GAA | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-347_730-346ins others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449955 | |||||
| chr3:133449961
|
AAG | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0137others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-338_730-337del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449961 | |||||
| chr3:133449963
|
G | GAAGGAA | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0042others(1): Show | 4 | HG01167.hp2 HG01169.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449963 | |||||
| chr3:133449963
|
G | GAAGGAAA others(3): Show |
16 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0051others(13): Show | 16 | HG00423.hp2 HG00621.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449963 | |||||
| chr3:133449964
|
A | AAG | 18 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(15): Show | 21 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | ||||||
| chr3:133449964
|
A | AAGGAAAG others(8): Show |
11 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | ||||||
| chr3:133449964
|
A | AAGGAAAG others(12): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0068a0002c0003t0001g0220others(1): Show | 4 | HG00099.hp2 HG01175.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(19): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | ||||||
| chr3:133449968
|
A | AG | 18 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0045others(15): Show | 18 | HG00423.hp2 HG00621.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.730-334dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449968 | |||||
| chr3:133449968
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0027others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.730-335A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449968 | ||||||
| chr3:133449969
|
G | GA | 5 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0070others(2): Show | 5 | HG02630.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-332dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449969 | |||||
| chr3:133449972
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0015others(14): Show | 18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.730-331G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449972 | ||||||
| chr3:133449972
|
G | T | 4 | a0001c0002t0001g0037a0001c0002t0001g0088a0001c0002t0001g0203others(1): Show | 4 | HG00735.hp2 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-331G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449972 | ||||||
| chr3:133449976
|
A | AG | 4 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0260others(1): Show | 6 | HG01255.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-326dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449976 | |||||
| chr3:133449976
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.730-327A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449976 | ||||||
| chr3:133449978
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0029others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.730-325A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449978 | ||||||
| chr3:133449978
|
AAGGAAAG others(9): Show |
A | 4 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0143others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-323_730-308del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449978 | |||||
| chr3:133449980
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(31): Show | 35 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.730-323G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449980 | ||||||
| chr3:133449982
|
A | AAAGG | 17 | a0001c0001t0001g0104a0001c0001t0001g0265a0001c0002t0001g0031others(14): Show | 17 | HG00423.hp1 HG00621.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.730-287_730-284dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(1): Show |
48 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0144others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.730-291_730-284dup others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(5): Show |
34 | a0001c0001t0001g0113a0001c0001t0001g0152a0001c0001t0001g0169others(31): Show | 35 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.730-295_730-284dup others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(9): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0073others(14): Show | 17 | HG00099.hp1 HG01243.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-299_730-284dup others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(13): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0072others(3): Show | 6 | HG01081.hp1 HG01346.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-303_730-284dup others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(17): Show |
6 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0147others(3): Show | 7 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-307_730-284dup others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(25): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0212 | 2 | HG01928.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.730-315_730-284dup others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(29): Show |
1 | a0004c0005t0001g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.730-319_730-284dup others(36): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAAGGAAG others(33): Show |
1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.730-284_730-283ins others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AAGG | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0018others(39): Show | 44 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.730-320_730-319ins others(3): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
A | AGGAAGGA others(3): Show |
1 | a0001c0002t0001g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.730-321_730-320ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449982 | ||||||
| chr3:133449982
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0015others(13): Show | 17 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-321A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449982 | ||||||
| chr3:133449982
|
AAAGGAAG others(5): Show |
A | 5 | a0001c0001t0001g0135a0001c0001t0001g0149a0001c0001t0001g0176others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-295_730-284del others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449982
|
AAAGGAAG others(9): Show |
A | 5 | a0001c0002t0001g0058a0001c0002t0001g0085a0001c0002t0001g0086others(2): Show | 5 | HG01070.hp2 HG01074.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-299_730-284del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | |||||
| chr3:133449986
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730-317G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449986 | ||||||
| chr3:133449998
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0143others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-305G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449998 | ||||||
| chr3:133450016
|
A | AGGAAGGA others(17): Show |
1 | a0001c0001t0001g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.730-284_730-283ins others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | |||||
| chr3:133450016
|
A | AGGAAGGA others(9): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0160a0001c0001t0001g0162others(2): Show | 5 | HG01123.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-284_730-283ins others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | |||||
| chr3:133450016
|
A | AGGAAGGA others(5): Show |
5 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0161others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-284_730-283ins others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | |||||
| chr3:133450016
|
A | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(75): Show | 79 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.730-287A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450016 | ||||||
| chr3:133450056
|
AAGAG | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0149others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-241_730-238del others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450056 | |||||
| chr3:133450237
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0020 | 2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.730-66T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450237 | ||||||
| chr3:133450283
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730-20A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450283 | ||||||
| chr3:133450296
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | NA18956.hp2 NA18972.hp2 NA19085.hp1 |
splice_region_variant&intron_variant | LOW | c.730-7T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450296 | ||||||
| chr3:133450477
|
A | G | 1 | a0005c0006t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.891+13A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450477 | ||||||
| chr3:133450781
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.891+317C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450781 | ||||||
| chr3:133450843
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0239 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.891+379A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450843 | ||||||
| chr3:133450883
|
G | A | 96 | a0001c0002t0001g0016a0001c0002t0001g0035a0001c0002t0001g0037others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.891+419G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450883 | ||||||
| chr3:133450988
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450988 | ||||||
| chr3:133451110
|
C | CA | 189 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.891+665dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | |||||
| chr3:133451110
|
C | CAA | 41 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(38): Show | 43 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.891+664_891+665dup others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | |||||
| chr3:133451110
|
CA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0149others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+665delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | |||||
| chr3:133451185
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0133others(2): Show | 5 | HG01884.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+721A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451185 | ||||||
| chr3:133451223
|
A | G | 1 | a0001c0002t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.891+759A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451223 | ||||||
| chr3:133451254
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.891+790A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451254 | ||||||
| chr3:133451276
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.891+812T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451276 | ||||||
| chr3:133451313
|
CATA | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0075others(13): Show | 16 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.891+853_891+855del others(3): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451313 | |||||
| chr3:133451321
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.891+857G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451321 | ||||||
| chr3:133451377
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(95): Show | 100 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.891+913A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451377 | ||||||
| chr3:133451386
|
G | A | 1 | a0002c0003t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.891+922G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451386 | ||||||
| chr3:133451514
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0032others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+1050C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451514 | ||||||
| chr3:133451592
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.891+1128T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451592 | ||||||
| chr3:133451845
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0204a0001c0001t0001g0224 | 3 | HG01952.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.891+1381T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451845 | ||||||
| chr3:133451893
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.891+1429A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451893 | ||||||
| chr3:133452315
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0147others(2): Show | 6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+1851C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452315 | ||||||
| chr3:133452440
|
C | A | 97 | a0001c0001t0001g0093a0001c0002t0001g0016a0001c0002t0001g0035others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.891+1976C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452440 | ||||||
| chr3:133452458
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0249 | 3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.891+1994C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452458 | ||||||
| chr3:133452515
|
T | G | 106 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(103): Show | 107 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.891+2051T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452515 | ||||||
| chr3:133452583
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+2119A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452583 | ||||||
| chr3:133452661
|
C | G | 73 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 74 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.891+2197C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452661 | ||||||
| chr3:133452898
|
A | T | 108 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 109 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.891+2434A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452898 | ||||||
| chr3:133453079
|
G | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.891+2615G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453079 | ||||||
| chr3:133453347
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.891+2883C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453347 | ||||||
| chr3:133453350
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.891+2886T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453350 | ||||||
| chr3:133453517
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+3053C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453517 | ||||||
| chr3:133453530
|
C | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 109 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.891+3066C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453530 | ||||||
| chr3:133453602
|
A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 101 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.891+3138A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453602 | ||||||
| chr3:133453788
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0239 | 3 | HG02451.hp2 HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.891+3324C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453788 | ||||||
| chr3:133453861
|
T | A | 21 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0061others(18): Show | 21 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.891+3397T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453861 | ||||||
| chr3:133453869
|
T | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+3405T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453869 | ||||||
| chr3:133453906
|
C | T | 19 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0071others(16): Show | 19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.891+3442C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453906 | ||||||
| chr3:133453923
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0022others(117): Show | 121 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.891+3459T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453923 | ||||||
| chr3:133453965
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0022others(19): Show | 23 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.891+3501G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453965 | ||||||
| chr3:133454213
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0155 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.891+3749A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454213 | ||||||
| chr3:133454352
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.891+3888T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454352 | ||||||
| chr3:133454359
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0161a0001c0001t0001g0165 | 3 | HG02559.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.891+3895T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454359 | ||||||
| chr3:133454506
|
A | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.891+4042A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454506 | ||||||
| chr3:133454520
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+4056G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454520 | ||||||
| chr3:133454559
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.891+4095C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454559 | ||||||
| chr3:133454749
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+4285C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454749 | ||||||
| chr3:133454813
|
T | A | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.891+4349T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454813 | ||||||
| chr3:133454831
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0161others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+4367A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454831 | ||||||
| chr3:133454885
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.891+4421G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454885 | ||||||
| chr3:133455148
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(222): Show | 230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.891+4684T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455148 | ||||||
| chr3:133455208
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+4744A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455208 | ||||||
| chr3:133455223
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+4759C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455223 | ||||||
| chr3:133455309
|
G | T | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.891+4845G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455309 | ||||||
| chr3:133455335
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 103 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.891+4871C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455335 | ||||||
| chr3:133455605
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(63): Show | 68 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.891+5141C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455605 | ||||||
| chr3:133455654
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0022others(117): Show | 121 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.891+5190T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455654 | ||||||
| chr3:133455705
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0024others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5241A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455705 | ||||||
| chr3:133455806
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0164a0001c0004t0001g0034 | 3 | HG01123.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891+5342G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455806 | ||||||
| chr3:133455991
|
C | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0160 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.891+5527C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455991 | ||||||
| chr3:133456405
|
T | A | 1 | a0001c0002t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.891+5941T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456405 | ||||||
| chr3:133456425
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.891+5961T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456425 | ||||||
| chr3:133456437
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.891+5973G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456437 | ||||||
| chr3:133456459
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(33): Show | 38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+5995G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456459 | ||||||
| chr3:133456473
|
G | C | 1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.891+6009G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456473 | ||||||
| chr3:133456527
|
G | A | 2 | a0001c0002t0001g0054a0001c0002t0001g0096 | 2 | NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.891+6063G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456527 | ||||||
| chr3:133456548
|
A | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0237a0001c0001t0001g0238others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+6084A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456548 | ||||||
| chr3:133456576
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.891+6112G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456576 | ||||||
| chr3:133456616
|
T | A | 16 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0071others(13): Show | 16 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6152T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456616 | ||||||
| chr3:133456801
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+6337A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456801 | ||||||
| chr3:133456918
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0199 | 2 | HG02129.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.891+6454A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456918 | ||||||
| chr3:133456940
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0020 | 2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.891+6476T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456940 | ||||||
| chr3:133456994
|
C | CT | 16 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0071others(13): Show | 16 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6534dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133456994 | |||||
| chr3:133457118
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0159 | 2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.891+6654G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457118 | ||||||
| chr3:133457493
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0241 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.891+7029A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457493 | ||||||
| chr3:133457556
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0147others(2): Show | 6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+7092A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457556 | ||||||
| chr3:133457558
|
T | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 60 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.891+7094T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457558 | ||||||
| chr3:133457631
|
G | C | 1 | a0001c0002t0001g0186 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.891+7167G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457631 | ||||||
| chr3:133457688
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0160 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.891+7224A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457688 | ||||||
| chr3:133457728
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+7264T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457728 | ||||||
| chr3:133457729
|
C | T | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.891+7265C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457729 | ||||||
| chr3:133457911
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.891+7447T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457911 | ||||||
| chr3:133457953
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0161others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+7489A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457953 | ||||||
| chr3:133458004
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0147others(2): Show | 6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+7540A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458004 | ||||||
| chr3:133458326
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.891+7862T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458326 | ||||||
| chr3:133458492
|
A | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(33): Show | 38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+8028A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458492 | ||||||
| chr3:133458504
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+8040G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458504 | ||||||
| chr3:133458519
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.891+8055C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458519 | ||||||
| chr3:133458662
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.892-8166C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458662 | ||||||
| chr3:133458724
|
C | G | 2 | a0001c0002t0001g0028a0001c0002t0001g0053 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.892-8104C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458724 | ||||||
| chr3:133458840
|
C | T | 1 | a0002c0007t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.892-7988C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458840 | ||||||
| chr3:133458918
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.892-7910G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458918 | ||||||
| chr3:133458922
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0161others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-7906G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458922 | ||||||
| chr3:133458969
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0161others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-7859C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458969 | ||||||
| chr3:133458988
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.892-7840G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458988 | ||||||
| chr3:133459011
|
C | T | 59 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.892-7817C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459011 | ||||||
| chr3:133459104
|
C | T | 37 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.892-7724C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459104 | ||||||
| chr3:133459304
|
G | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0025others(117): Show | 121 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.892-7524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459304 | ||||||
| chr3:133459427
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0155 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-7401T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459427 | ||||||
| chr3:133459588
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.892-7240C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459588 | ||||||
| chr3:133459656
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0129others(1): Show | 6 | HG01255.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-7172C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459656 | ||||||
| chr3:133459678
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892-7150T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459678 | ||||||
| chr3:133459723
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.892-7105C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459723 | ||||||
| chr3:133460360
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0223 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.892-6468C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460360 | ||||||
| chr3:133460586
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0249 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.892-6242C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460586 | ||||||
| chr3:133460675
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0147 | 3 | HG01884.hp2 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.892-6153C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460675 | ||||||
| chr3:133460736
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0036others(93): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.892-6092C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460736 | ||||||
| chr3:133460760
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.892-6068A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460760 | ||||||
| chr3:133461089
|
G | A | 29 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 29 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.892-5739G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461089 | ||||||
| chr3:133461113
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.892-5715C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461113 | ||||||
| chr3:133461329
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.892-5499G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461329 | ||||||
| chr3:133461413
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-5415C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461413 | ||||||
| chr3:133461493
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 275 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.892-5335C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461493 | ||||||
| chr3:133461605
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-5223A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461605 | ||||||
| chr3:133461631
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0146others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-5197A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461631 | ||||||
| chr3:133461657
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0267 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.892-5171T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461657 | ||||||
| chr3:133462036
|
G | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.892-4792G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462036 | ||||||
| chr3:133462071
|
TG | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.892-4755delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133462071 | |||||
| chr3:133462073
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.892-4755G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462073 | ||||||
| chr3:133462153
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0143 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-4675G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462153 | ||||||
| chr3:133462161
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0155 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-4667G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462161 | ||||||
| chr3:133462226
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 46 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.892-4602C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462226 | ||||||
| chr3:133462247
|
T | TA | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(100): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-4574dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133462247 | |||||
| chr3:133462251
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-4577A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462251 | ||||||
| chr3:133462302
|
T | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0152a0001c0001t0001g0223others(11): Show | 15 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-4526T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462302 | ||||||
| chr3:133462420
|
G | T | 1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.892-4408G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462420 | ||||||
| chr3:133462492
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0112a0001c0001t0001g0258 | 3 | HG02630.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.892-4336G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462492 | ||||||
| chr3:133462544
|
C | T | 4 | a0001c0002t0001g0039a0001c0002t0001g0088a0001c0002t0001g0215others(1): Show | 4 | HG00099.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-4284C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462544 | ||||||
| chr3:133462740
|
A | G | 1 | a0001c0002t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.892-4088A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462740 | ||||||
| chr3:133462767
|
T | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 46 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.892-4061T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462767 | ||||||
| chr3:133462981
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0027 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.892-3847A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462981 | ||||||
| chr3:133463034
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.892-3794T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463034 | ||||||
| chr3:133463081
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892-3747G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463081 | ||||||
| chr3:133463092
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(100): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-3736T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463092 | ||||||
| chr3:133463106
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.892-3722C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463106 | ||||||
| chr3:133463243
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.892-3585A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463243 | ||||||
| chr3:133463300
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 70 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.892-3528A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463300 | ||||||
| chr3:133463460
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.892-3368C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463460 | ||||||
| chr3:133463573
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.892-3255A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463573 | ||||||
| chr3:133463855
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0155 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-2973C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463855 | ||||||
| chr3:133463869
|
C | G | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.892-2959C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463869 | ||||||
| chr3:133463913
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.892-2915C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463913 | ||||||
| chr3:133464031
|
C | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(15): Show | 19 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-2797C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464031 | ||||||
| chr3:133464080
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.892-2748G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464080 | ||||||
| chr3:133464623
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(100): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-2205T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464623 | ||||||
| chr3:133464661
|
T | TAC | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.892-2166_892-2165i others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133464661 | |||||
| chr3:133464663
|
G | T | 1 | a0002c0007t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.892-2165G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464663 | ||||||
| chr3:133464705
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.892-2123G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464705 | ||||||
| chr3:133464908
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.892-1920G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464908 | ||||||
| chr3:133465001
|
C | CT | 6 | a0001c0001t0001g0179a0001c0001t0001g0228a0001c0002t0001g0031others(3): Show | 6 | HG02071.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-1809dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133465001 | |||||
| chr3:133465001
|
CT | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0152others(15): Show | 19 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-1809delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133465001 | |||||
| chr3:133465163
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.892-1665C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465163 | ||||||
| chr3:133465427
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0146others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-1401T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465427 | ||||||
| chr3:133465476
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0224 | 2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.892-1352G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465476 | ||||||
| chr3:133465540
|
T | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.892-1288T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465540 | ||||||
| chr3:133465708
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.892-1120G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465708 | ||||||
| chr3:133465867
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-961C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465867 | ||||||
| chr3:133465887
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0138 | 3 | HG02109.hp1 HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.892-941T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465887 | ||||||
| chr3:133466009
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.892-819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466009 | ||||||
| chr3:133466047
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0143 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-781G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466047 | ||||||
| chr3:133466088
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(100): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-740G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466088 | ||||||
| chr3:133466158
|
AC | A | 7 | a0001c0001t0001g0083a0001c0001t0001g0123a0001c0001t0001g0127others(4): Show | 7 | HG02015.hp1 HG02071.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-668delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466158 | |||||
| chr3:133466167
|
C | CG | 149 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.892-653dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466167 | |||||
| chr3:133466406
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0143 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-422G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466406 | ||||||
| chr3:133466429
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.892-399T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466429 | ||||||
| chr3:133466450
|
C | T | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 98 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.892-378C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466450 | ||||||
| chr3:133466661
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.892-167C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466661 | ||||||
| chr3:133466677
|
C | CAAAAAAA others(2): Show |
42 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(39): Show | 44 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.892-139_892-131dup others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(3): Show |
53 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0025others(50): Show | 53 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.892-140_892-131dup others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(4): Show |
22 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0029others(19): Show | 22 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-141_892-131dup others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.892-142_892-131dup others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(7): Show |
47 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0036others(44): Show | 48 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.892-144_892-131dup others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(8): Show |
35 | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0103others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.892-145_892-131dup others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(9): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0257a0001c0002t0001g0048others(7): Show | 10 | HG01169.hp2 HG01952.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-146_892-131dup others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(10): Show |
9 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0065others(6): Show | 9 | HG00738.hp1 HG01243.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-147_892-131dup others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466677
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.892-148_892-131dup others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | |||||
| chr3:133466701
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0001g0222 | 2 | HG00735.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.892-127G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466701 | ||||||
| chr3:133466811
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0261 | 2 | HG00738.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892-17G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466811 | ||||||
| chr3:133466814
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.892-14C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466814 | ||||||
| chr3:133466990
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1023+31T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133466990 | ||||||
| chr3:133467004
|
ACT | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1023+50_1023+51del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 133467004 | |||||
| chr3:133467158
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(33): Show | 36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023+199C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467158 | ||||||
| chr3:133467215
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1023+256G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467215 | ||||||
| chr3:133467304
|
G | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1023+345G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467304 | ||||||
| chr3:133467322
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+363G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467322 | ||||||
| chr3:133467375
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0004t0001g0033 | 5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+416T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467375 | ||||||
| chr3:133467420
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1023+461C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467420 | ||||||
| chr3:133467569
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+610T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467569 | ||||||
| chr3:133467664
|
C | T | 8 | a0001c0002t0001g0035a0001c0002t0001g0047a0001c0002t0001g0048others(5): Show | 8 | HG00558.hp1 HG00597.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+705C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467664 | ||||||
| chr3:133467841
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1023+882C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467841 | ||||||
| chr3:133467897
|
G | T | 95 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 96 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1023+938G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467897 | ||||||
| chr3:133467984
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1023+1025A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467984 | ||||||
| chr3:133468058
|
G | A | 2 | a0001c0001t0001g0177a0001c0004t0001g0034 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1023+1099G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468058 | ||||||
| chr3:133468096
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+1137A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468096 | ||||||
| chr3:133468128
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 32 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+1169T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468128 | ||||||
| chr3:133468155
|
C | A | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1023+1196C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468155 | ||||||
| chr3:133468169
|
TCCCTGCC others(19): Show |
T | 1 | a0001c0001t0001g0240 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1023+1211_1023+123 others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468169 | ||||||
| chr3:133468172
|
C | G | 1 | a0001c0002t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1023+1213C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468172 | ||||||
| chr3:133468293
|
C | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 31 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1023+1334C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468293 | ||||||
| chr3:133468321
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1023+1362G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468321 | ||||||
| chr3:133468469
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 32 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+1510T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468469 | ||||||
| chr3:133468572
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+1613G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468572 | ||||||
| chr3:133468596
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(15): Show | 19 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1023+1637T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468596 | ||||||
| chr3:133468616
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1023+1657G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468616 | ||||||
| chr3:133468735
|
A | G | 1 | a0001c0002t0001g0193 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1023+1776A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468735 | ||||||
| chr3:133469035
|
G | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0146others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1023+2076G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469035 | ||||||
| chr3:133469203
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1023+2244A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469203 | ||||||
| chr3:133469220
|
G | A | 1 | a0001c0002t0001g0243 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1023+2261G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469220 | ||||||
| chr3:133469224
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1023+2265C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469224 | ||||||
| chr3:133469440
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1023+2481T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469440 | ||||||
| chr3:133469541
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0267 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1023+2582T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469541 | ||||||
| chr3:133469936
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0136others(6): Show | 10 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1024-2409C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469936 | ||||||
| chr3:133470018
|
CT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(96): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-2324delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 133470018 | |||||
| chr3:133470188
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(96): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-2157G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470188 | ||||||
| chr3:133470193
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0130others(5): Show | 8 | HG01123.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024-2152G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470193 | ||||||
| chr3:133470348
|
T | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 112 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.1024-1997T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470348 | ||||||
| chr3:133470472
|
A | G | 72 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1024-1873A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470472 | ||||||
| chr3:133470558
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0143 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1024-1787G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470558 | ||||||
| chr3:133470596
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1024-1749G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470596 | ||||||
| chr3:133470692
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1024-1653A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470692 | ||||||
| chr3:133470871
|
A | C | 2 | a0001c0001t0001g0118a0001c0002t0001g0126 | 2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1024-1474A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470871 | ||||||
| chr3:133470887
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1024-1458C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470887 | ||||||
| chr3:133470888
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0155 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1024-1457G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470888 | ||||||
| chr3:133470905
|
G | C | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1024-1440G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470905 | ||||||
| chr3:133470919
|
G | A | 2 | a0001c0001t0001g0005a0001c0002t0001g0270 | 2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1024-1426G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470919 | ||||||
| chr3:133471285
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1024-1060G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471285 | ||||||
| chr3:133471346
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(96): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-999C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471346 | ||||||
| chr3:133471487
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0130others(5): Show | 8 | HG01123.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024-858C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471487 | ||||||
| chr3:133471520
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0112a0001c0001t0001g0144others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024-825T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471520 | ||||||
| chr3:133471747
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1024-598G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471747 | ||||||
| chr3:133471921
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1024-424G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471921 | ||||||
| chr3:133472033
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1024-312C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472033 | ||||||
| chr3:133472102
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1024-243C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472102 | ||||||
| chr3:133472249
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(132): Show | 139 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.1024-96A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472249 | ||||||
| chr3:133472609
|
A | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 157 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1244+44A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472609 | ||||||
| chr3:133472639
|
C | G | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1244+74C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472639 | ||||||
| chr3:133472663
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0129others(1): Show | 6 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+98C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472663 | ||||||
| chr3:133472743
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0177 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1244+178A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472743 | ||||||
| chr3:133472772
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1244+207T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472772 | ||||||
| chr3:133472829
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0249 | 3 | HG01175.hp1 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1244+264G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472829 | ||||||
| chr3:133472932
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0249 | 3 | HG01175.hp1 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1244+367C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472932 | ||||||
| chr3:133472951
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0030others(4): Show | 7 | HG00738.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+400dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133472951 | |||||
| chr3:133472991
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1244+426T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472991 | ||||||
| chr3:133473153
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0027 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1244+588T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473153 | ||||||
| chr3:133473232
|
C | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0136others(7): Show | 11 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1244+667C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473232 | ||||||
| chr3:133473255
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0241 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1244+690C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473255 | ||||||
| chr3:133473325
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 205 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1244+760C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473325 | ||||||
| chr3:133473438
|
C | CA | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 148 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1244+894dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | |||||
| chr3:133473438
|
C | CAA | 25 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0052others(22): Show | 25 | HG00621.hp2 HG00738.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1244+893_1244+894d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | |||||
| chr3:133473438
|
CA | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 22 | HG01123.hp2 HG01175.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1244+894delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | |||||
| chr3:133473482
|
A | T | 9 | a0001c0001t0001g0068a0002c0003t0001g0003a0002c0003t0001g0115others(6): Show | 10 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+917A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473482 | ||||||
| chr3:133473579
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0155a0001c0002t0001g0031others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244+1014G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473579 | ||||||
| chr3:133473633
|
A | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0136a0001c0001t0001g0140others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+1068A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473633 | ||||||
| chr3:133473675
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1244+1110G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473675 | ||||||
| chr3:133473710
|
A | G | 1 | a0006c0009t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244+1145A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473710 | ||||||
| chr3:133473745
|
G | A | 2 | a0001c0002t0001g0066a0001c0002t0001g0088 | 2 | HG03942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244+1180G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473745 | ||||||
| chr3:133473773
|
G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1196G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473773 | ||||||
| chr3:133473774
|
G | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1195G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473774 | ||||||
| chr3:133473775
|
G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1194G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473775 | ||||||
| chr3:133473776
|
T | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1193T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473776 | ||||||
| chr3:133473778
|
A | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1191A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473778 | ||||||
| chr3:133473781
|
T | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1188T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473781 | ||||||
| chr3:133473782
|
C | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1187C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473782 | ||||||
| chr3:133473787
|
G | A | 101 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0040others(98): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1245-1182G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473787 | ||||||
| chr3:133474222
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0030others(4): Show | 7 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245-747T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474222 | ||||||
| chr3:133474332
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1245-637C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474332 | ||||||
| chr3:133474398
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0241 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1245-571T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474398 | ||||||
| chr3:133474468
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0030others(4): Show | 7 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245-501A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474468 | ||||||
| chr3:133474556
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0241 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1245-413T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474556 | ||||||
| chr3:133474568
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(146): Show | 152 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1245-401A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474568 | ||||||
| chr3:133474646
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1245-323T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474646 | ||||||
| chr3:133474690
|
C | A | 1 | a0001c0002t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1245-279C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474690 | ||||||
| chr3:133474693
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0155a0001c0002t0001g0031others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245-276A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474693 | ||||||
| chr3:133474713
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0020others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1245-256T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474713 |